Optical-acoustic imaging device

Information

  • Patent Grant
  • 9532766
  • Patent Number
    9,532,766
  • Date Filed
    Friday, December 19, 2014
    9 years ago
  • Date Issued
    Tuesday, January 3, 2017
    7 years ago
Abstract
The present invention is a guide wire imaging device for vascular or non-vascular imaging utilizing optic acoustical methods, which device has a profile of less than 1 mm in diameter. The ultrasound imaging device of the invention comprises a single mode optical fiber with at least one Bragg grating, and a piezoelectric or piezo-ceramic jacket, which device may achieve omnidirectional (360°) imaging. The imaging guide wire of the invention can function as a guide wire for vascular interventions, can enable real time imaging during balloon inflation, and stent deployment, thus will provide clinical information that is not available when catheter-based imaging systems are used. The device of the invention may enable shortened total procedure times, including the fluoroscopy time, will also reduce radiation exposure to the patient and to the operator.
Description
II. FIELD OF THE INVENTION

The present invention relates to an omnidirectional imaging device for vascular or nonvascular imaging that may be used as an intravascular guidewire.


III. BACKGROUND OF THE INVENTION

Intra-vascular and non-vascular imaging are very important techniques that provide information that is not available by angiographic imaging methods such as information about the composition of the subject vessel wall, plaque analysis, and disease processes. It is also very important as an aid to vascular interventions, especially stent deployment.


Prior art intra-vascular ultrasound (IVUS) devices are described as generally adapted to be used via catheter, and are primarily either mechanical or solid state. In the mechanical IVUS catheter, image scanning is accomplished by a rotating drive shaft causing mechanical rotation of a miniature acoustical transmitter. The drive shaft and most of the transmitter are located within the body of a flexible catheter. The design of these devices generally creates difficulties in tracking with a limited image area, and vibration of the catheter during rotation poses a risk to the patient of arterial spasm.


The solid state IVUS catheter does not have a rotating driveshaft, but rather produces images by scanning with electrical impulses that are generated from a large number of piezoelectric elements located within the IVUS. Each piezoelectric element is controlled by a driver such as a computer. Conventional solid state IVUS devices generally have a lumen adapted to receive a guidewire, and a coaxial cable design which enhances the trackability and pushability of the device as compared to the mechanical model.


One deficiency in conventional mechanical and solid state IVUS catheters is the external diameter, generally approximately 1.2 mm. Mechanical limitations on component sizes and noise effects have thus far limited commercially feasible manufacture of a smaller diameter device. In addition, both these devices must be used with traditional intraluminal catherization methods, that is, with the catheter situated over a guidewire.


Some prior art ultrasonic catheter patents describe a thin films of a flexible piezoelectric plastic material, such as poled polyvinyldiene fluoride (PVDF), which can be spot polarized in active regions to serve as piezoelectric transducers. In these devices, the PVDF film is used both as a transmitter and as a receiver. However, it is difficult to adapt this technology to small (less than 1.2 mm diameter) imaging catheters with multiple elements, for several reasons. One such reason is the very low electrical capacitor of each of the receiver elements having a small surface area as compared to the capacitor of the long electrode conductors (more then 1 m long). This relationship of elements in the device generally results in a low signal/noise relation. While the signal to noise ration may be increased by the use of preamplifiers near the receivers, physically accommodating the preamplifiers inside of a space with an outer diameter of less than 1.2 mm is very difficult. Another reason is the large signal cross talk experienced due to the long, closely clustered conductors within the device.


Other relevant prior art technology that couples ultrasonic waves with an optical fiber in an intravascular device includes a transducer which is precisely located on thin slab of piezoelectric material. The transducer generates ultrasonic acoustic surface waves that propagate on the surface or within the bulk of the slab. These devices are limited, however, in that they generate doppler signals and not images, and their probing range is limited to the area just in front of the catheter pass. Also, the piezoelectric chip is not small enough to be used in a device with a profile diameter of less than 1 mm, and more importantly, less than 0.5 mm.


In most commercially available piezoceramic and PVDF IVUS devices, one significant problem is the difficulty in constructing ultrasound imaging catheters with a diameter of less then approx. 1 mm, and where the signal to noise ratio will be high enough for the device to be easily used. Such devices are also difficult to manufacture from a mechanical perspective, using conventional components.


Accordingly, it would be useful to have an intra-vascular ultrasound imaging device with a profile of less that approximately 1 mm in diameter and most preferably less than 0.5 mm in diameter, with a signal/noise ratio that is higher than those generated by conventional IVUS devices such as those described above. It would also be useful to have an imaging device for non-vascular applications which demand a device profile of less than 1 mm.


IV. SUMMARY OF THE INVENTION

The present invention is a guidewire imaging device for vascular or non-vascular imaging utilizing optico-acoustical methods, which device has a profile of less than 1 mm in diameter, and most preferably less than 0.5 mm in diameter. The imaging device of the invention comprises a single-mode optical fiber with at least one Bragg grating and a piezoelectric or piezoceramic jacket, which device may achieve omnidirectional (360°) imaging. The imaging guidewire of the invention can function as the guidewire for vascular interventions, and can enables real time imaging during balloon inflation and stent deployment, thus will provide clinical information that is not available when catheter-based imaging systems are used. The device of the invention may enable shortened total procedure times, including the fluoroscopy time, and will also reduce radiation exposure to the patient and the operator.


Thus, it is an object of the invention to provide an optico-acoustic device for vascular or non-vascular imaging with a profile of less than 1 mm, and most preferably less than 0.5 mm.


Another object of the invention is to provide a guidewire imaging device for producing real time images during vascular intervention procedures prior to catheter insertion and throughout the procedure.


A further object of the invention is to provide a device which is capable of omnidirectional 360 degree imaging.


Still another object of the invention is to provide an intravascular imaging technique with an improved signal to noise ratio over prior art intravascular imaging devices.





V. DESCRIPTION OF THE FIGURES


FIG. 1 is a schematic diagram of a conventional optical fiber.



FIG. 2 is schematic diagram of a PVDF jacketed optical fiber.



FIG. 3 is a schematic diagram of a Fiber Bragg Grating based sensor.



FIG. 4 is a schematic depiction of a PVDF and FBG based ultrasound pulser-receiver of the invention.



FIG. 5 is a schematic diagram of a PVDF and FBG based ultrasound pulser-receiver having a plurality of Bragg gratings.



FIG. 6 is a schematic diagram of a PVDF and FBG based ultrasound pulser-receiver having a plurality of variable Bragg gratings.



FIG. 7 is a schematic depiction of the optical fiber of the invention with a strength member.



FIG. 8 is a schematic depiction of an ultrasound imaging catheter of the invention.



FIG. 9 is a schematic depiction of a catheter of the invention provided with a spiral strength member.



FIG. 10 is a schematic depiction of a fiber with bead-shaped cladding.



FIG. 11 is a schematic depiction of a fiber of the invention with bead cladding and with a spiral strength member.



FIG. 12 is a device of the invention with bead cladding and with ribs.



FIG. 13 is a catheter of the invention adapted with lens apertures.





VI. DESCRIPTION OF THE PREFERRED EMBODIMENTS

The device of the invention utilizes a single optical fiber, for example but not limited to a glass fiber at least partly composed of silicon dioxide. The basic structure of a generic optical fiber is illustrated in FIG. 2, which fiber generally consists of layered glass cylinders. There is a central cylinder called the core 1. Surrounding this is a cylindrical shell of glass, possibly multilayered, called the cladding 2. This cylinder is surrounded by some form of protective jacket 3, usually of plastic (such as acrylate). For protection from the environment and more mechanical strength than jackets alone provide, fibers are commonly incorporated into cables. Typical cables have a polyethylene sheath 4 that encases the fibers within a strength member 5 such as steel or Kevlar strands.


Optical fibers can be broadly classified according to their refractive index profile and dimensions. The invention described below uses single-mode fibers.



FIG. 2 shows an optical fiber coated by a piezoelectric jacket, to which an alternating voltage electrical generator 6 is attached to electrodes 32 situated on either side of the jacket. the generator 6 sends electrical impulses to the electrodes 32, which impulses cause mechanical oscillations in the jacket 31.


In recent years Fiber Bragg Grating (FBG) sensors have generated great interest because of their potential use in a wide range of applications such as telecommunications. FBGs form an integral part of the optical fiber structure and can be written intracore during manufacture or after manufacture.


As illustrated in FIG. 3, when illuminated by a broadband light laser 7, a uniform pitch Fiber Bragg Grating (“FBG”) element 8 will reflect back a narrowband component centered about the Bragg wavelength λ given by λ=2nΛ, where n is the index of the core of the fiber and Λ represents the grating period. Using a tunable laser 7 and different grating periods (each period is approximately 0.5 μ) situated in different positions on the fiber, it is possible to make independent measurement in each of the grating positions.


EXAMPLE 1

One preferred embodiment of the invention is illustrated in FIG. 4. This embodiment includes a single-mode optical fiber with a Bragg grating 8 and a piezoelectric or piezoceramic jacket 31. The jacket may be any suitable piezoelectric or piezoceramic material, and one preferable material is poled PVDF. It is contemplated that other jacket materials will work with the invention, so long as the material has suitable flexibility and piezoelectric characteristics.


In the preferred embodiment of the device of the invention as illustrated in FIG. 4, an electrical generator 6 transmits ultrasound impulses 10 to both the Bragg grating 8 and to the outer medium 13 in which the device is located, for example, the blood. Primary and reflected impulses 11 are received by the Bragg grating 8 and recorded by electronic instruments 9 using conventional methods, such as by a photodetector and an oscilloscope. From the recorded signals, a corresponding image is generated by conventional methods. Hence, the invention utilizes omnidirectional sonar (pulser-receiver) at each of the imaging locations. If mechanical deformations appear inside the optical fiber, they cause modulation of light reflected backward, which is received by the electronic instruments 9.


It is contemplated that in the various devices constructed according to the invention, the thickness of the jacket as well as the diameter of the optical fiber may vary significantly, and the only requirement is that the entire device be less than 1 mm and most preferably less than 300 μ, and that the signals generated by the device are suitable to generate an image.


The ultrasound transmitter device of the invention comprises a single fiber covered by a piezoelectric active (poled) PVDF jacket has a total outside diameter of preferably less than 1 mm, and most preferably less than 300 μ. It is also contemplated that devices may be made in accordance with the principles of the invention with profiles of approximately or less than 200 μ. Devices with other frequency transmitters may also be constructed in accordance with the principles of the invention, as applications dictate. The device of the invention includes any needed frequency of transmitter.


EXAMPLE 2

It may also be possible to expand the frequency band of the signal by using a damped silica fiber. In this variation of the preferred embodiment of the invention, frequency band expansion causes shortening of the signal in time, which improves the resolution of the received signal. For instance, using a damped fiber in a device of the invention, we have obtained maximum widths of the frequency band of the signal of approximately 110, although another variations will be achieved depending upon experimental conditions. If damped fibers are utilized, transmitters transmitting at less than 40 MHz may be used.


EXAMPLE 3

As shown in FIG. 5, one other preferred embodiment of an imaging device in accordance with the invention comprises a plurality of Bragg gratings 81 with different periods, each period being approximately 0.5 μ. By using multiple Bragg gratings, a set of distributed sonars are obtained. By utilizing a tunable laser 71 as previously described, we obtain scanning over an omnidirectional array. A Bragg grating length LB of some hundreds of optical wavelengths are sufficient to reflect considerable part of the optical beam. The ultrasound impulses 141 are received only by the Bragg gratings 81, with the period of Ai which is equal to the aperture Ax.


EXAMPLE 4

In yet another preferred embodiment of a device of the invention as illustrated in FIG. 6, instead of a plurality of Bragg gratings, the device may incorporate a single variable grating, with a variable period. When a tunable laser is adjusted to the wavelength λ1 the receiving element is the Bragg grating. When the laser wavelength is adjusted to other wavelengths λ2-6 . . . , the corresponding positioning of the Bragg grating along the axis of the fiber is also adjusted.


We have determined that for a device with a 40 MHz frequency transmitter and aperture Ax=151−200 μ, the reception obtained by the invention provides acceptable imaging.


EXAMPLE 5

In yet another preferred embodiment of the device of the invention as illustrated in FIG. 7, a strength member may be optionally added. This strength member is very thin, and even with the strength member, it is contemplated that the device of the invention is still less than 1 mm in diameter.


To preserve the omnidirectional scanning ability of the invention, the optical fiber is placed into the strength member 51 comprising a plurality of rectangular apertures 15. These apertures 15 have a length dimension 151 along axis x=Ax, and a circumferential dimension length 152=Aφö152. In a preferred embodiment the apertures are rectangular, although other shapes may be utilized. The apertures 15 may be distributed throughout the imaging portion of the device, and may be distributed in a pattern, for example a spiral as illustrated in FIG. 9.


EXAMPLE 6

Example 6, as illustrated in FIG. 8, is a catheter version of the device of the invention, which produces ultrasound scanning both along the axis and along the circumference. It is comprised of a single mode optical fiber 2 with a plurality of Bragg gratings 8. The optical fiber is provided with a jacket 3, and a strength member 51, which his set of apertures 15. The strength member may be made of any hard, flexible and durable biocompatible material such as metal. Apertures are placed uniformly on the surface of strength member, both along the length and angle. The outside diameter of this device is less than 1 mm, and most preferably less than 0.5 mm. It is contemplated that the device may further have a most preferred outer diameter of less than 400 μ. The apertures may be constructed using conventional photochemistry technology.


As illustrated in FIG. 8, the device is shown with an array of apertures Ax=Aφö=200 μ, period Ls=1000 μ. By applying electrical impulses to the electrodes of PVDF jacket 3 from electrical generator 6 we generate acoustical impulses in the all apertures simultaneously. The ultrasound impulses will expand in a direction perpendicular to the optical fiber surface, and reflect back from the nonhomogeneous medium (tissue). By tuning the laser 71, it is possible to realize scanning of the received ultrasound signals. Electronic instruments 9 receive, process and displaying the resulting images. One can estimate the scanning period Ls of scanning as 0.5 to 1.0 mm lengthwise and number of directions around the fiber as 5 to 10.


EXAMPLE 7

The design of the invention may also comprise more than one optical fiber. If there are a plurality of fibers within the strength member, it is possible to decrease the period and increase the number of directions of the scanning.


EXAMPLE 8


FIG. 9 shows a variation of the strength member 52, comprising a spiral strength member. Use of this member is believed to produce smoother scanning, and a simpler manufacture than a strength member with apertures.


EXAMPLE 9

As illustrated in FIG. 10, another variation of the device of the invention is a variable diameter cladding, preferably of silica, with a period L along the fiber. This variation is achieved by the use of beads 21, which causes an increased sensitivity to acoustical waves. Maximum efficiency is achieved if the period Lc is equal to one of the following resonance lengths: it is approximately equal to acoustical wavelength in water Lc1 Å (1500/40·106)=37.5·10−6 m (for 40 MHz); or it is equal to the quasi-Lamb wavelength in the silica fiber Lc2.


In this embodiment, the Bragg grating interacts with optical waves and with the acoustical grating formed by the beads.


EXAMPLE 10

As illustrated in FIG. 10, an additional increase in sensitivity f the device may optionally be received if a filler 16 is used to fill the gaps between the beads. This filler is produced from material with comparatively low acoustical impedance, such as a solid polymer, gel, fluid or other suitable material. For the purpose of yet additional increasing in sensitivity, gap filling filler is selected from the materials which sound velocity cf lower than sound velocity in water (blood), that is cf<1500 m/sec. One example of such materials is silicon rubber having the sound velocity cr—1000 m/sec. In consequence of the sound velocity difference the energy focusing is achieving. Thus, the filling material functions as a signal collecting lens.


EXAMPLE 11

Yet another variation of the device of the invention includes a spiral jacket 22, as shown in FIG. 11.


EXAMPLE 12

Another embodiment (illustrated in FIG. 12) includes adding ribs 23 to the jacket. In one example of a device with ribs, to achieve 40 MHz resonance, silica ribs should nave approximately dimensions: height Hr=10 microns and thickness Tr=4.5 microns. The oscillations of ribs 23 induce the additional deformations at the fiber axes, hence causing the increasing in sensitivity. It is possible to fabricate ribs by conventionally known micromachining technology.


In a deviation of the ribbed embodiment, the ribs may have varying thicknesses, which are believed to lead to acoustical damping, and hence an increase in bandwith and resolution. If each of the ribs 23 will have different height Hr and width Tr then they will resonate at different frequencies.


EXAMPLE 13

For the purpose of yet additional increases in sensitivity, the apertures of the strength member may filled with a material with a velocity cL>1500 m/sec, and an outside surface curvature which forms a focused lens, as illustrated in FIG. 13.


It is thus seen from the above description of the preferred embodiments that the objects of the invention are attained. Variations on this embodiment will be apparent to those skilled in the art without departing from the scope of the invention. All matter contained in the above description and the accompanying drawings is intended to be illustrative of the invention, and not limiting in the scope of the invention.

Claims
  • 1. A system for providing intravascular information, the system comprising: an intravascular guidewire configured to be introduced into a human or animal body, the guidewire having proximal and distal ends, and defining a longitudinal direction therebetween, the guidewire comprising: an optical fiber extending in the longitudinal direction, the optical fiber having a core; andat least one fiber Bragg grating sensor formed in the core of the optical fiber, wherein the fiber is capable of reflecting light after illuminating thereof by a tunable laser beam, the reflected light being defined by a wavelength having a period corresponding to that of an individual Bragg grating.
  • 2. The system of claim 1, wherein the optical fiber includes a plurality of optical fibers, wherein the at least one fiber Bragg sensor includes a plurality of fiber Bragg grating sensors, wherein individual fiber Bragg grating sensors are positioned at a plurality of separately addressable discrete locations on different ones of the optical fibers.
  • 3. The system of claim 2, wherein the separately addressable discrete locations are spaced apart from each other in the longitudinal direction.
  • 4. The system of claim 2, wherein the locations are distributed around a circumference of a distal portion of the guidewire.
  • 5. The system of claim 1, wherein the at least one fiber Bragg grating sensor includes a variable period.
  • 6. The system of claim 5, further including the tunable laser, optically coupled to the Bragg grating sensor including the variable period, the laser operable to adjust an effective location of the Bragg grating sensor by adjusting a wavelength of light to select a desired portion of the Bragg grating sensor that provides a corresponding desired period.
  • 7. The system of claim 1, wherein the guidewire is biocompatible and has a diameter of less than about 1 millimeter.
  • 8. The system of claim 1, wherein the optical fiber includes a cladding about at least a portion of the core, and in which a diameter of the cladding varies longitudinally along the guidewire.
  • 9. The system of claim 1, wherein the optical fiber includes a damped silica fiber.
  • 10. The system claim 1, wherein the optical fiber is a single-mode fiber.
I. RELATED APPLICATIONS

This application is a Continuation of U.S. application Ser. No. 12/020,736, filed on Jan. 28, 2008, now issued as U.S. Pat. No. 8,926,519, which is a Continuation of U.S. application Ser. No. 10/685,226, filed on Oct. 14, 2003, now issued as U.S. Pat. No. 7,527,594, which is a Continuation of U.S. application Ser. No. 09/623,248, filed on Jun. 11, 2002, now issued as U.S. Pat. No. 6,659,957, which is a National Stage filing under 35 U.S.C. 371 of PCT/US99/04913, filed on Mar. 5, 1999, published in English as WO 99/5059 on Nov. 18, 1999, which claims priority to U.S. Provisional Application No. 60/076,862, filed on Mar. 5, 1998, which applications and publications are incorporated herein by reference.

US Referenced Citations (195)
Number Name Date Kind
3995623 Blake et al. Dec 1976 A
4068191 Zemon et al. Jan 1978 A
4076379 Chouinard Feb 1978 A
4115753 Shajenko Sep 1978 A
4327738 Green et al. May 1982 A
4473065 Bates Sep 1984 A
4522193 Bates Jun 1985 A
4587972 Morantte, Jr. May 1986 A
4887605 Angelsen et al. Dec 1989 A
4900921 Spillman, Jr. Feb 1990 A
4917097 Proudian et al. Apr 1990 A
4946238 Sashin et al. Aug 1990 A
5007705 Morey et al. Apr 1991 A
5070882 Bui et al. Dec 1991 A
5095911 Pomeranz Mar 1992 A
5099090 Allan et al. Mar 1992 A
5109463 Lee Apr 1992 A
5135295 Jen et al. Aug 1992 A
5135486 Eberle et al. Aug 1992 A
5156772 Allan et al. Oct 1992 A
5167233 Eberle et al. Dec 1992 A
5178153 Einzig Jan 1993 A
5183048 Eberle Feb 1993 A
5186177 O'Donnell et al. Feb 1993 A
5226847 Thomas, III et al. Jul 1993 A
5240004 Walinsky et al. Aug 1993 A
5254112 Sinofsky et al. Oct 1993 A
5290275 Kittrell et al. Mar 1994 A
5305758 Dietz et al. Apr 1994 A
5325860 Seward et al. Jul 1994 A
5353262 Yakymyshyn et al. Oct 1994 A
5368037 Eberle et al. Nov 1994 A
5383467 Auer et al. Jan 1995 A
5400788 Dias et al. Mar 1995 A
5411500 Lafferty et al. May 1995 A
5427107 Milo et al. Jun 1995 A
5439000 Gunderson et al. Aug 1995 A
5453575 O'Donnell et al. Sep 1995 A
5469520 Morey et al. Nov 1995 A
5486170 Winston et al. Jan 1996 A
5493113 Dunphy et al. Feb 1996 A
5554139 Okajima Sep 1996 A
5558669 Reynard Sep 1996 A
5558699 Nakashima et al. Sep 1996 A
5573493 Sauer et al. Nov 1996 A
5582171 Chornenky et al. Dec 1996 A
5584793 Sauer et al. Dec 1996 A
5601087 Gunderson et al. Feb 1997 A
5603327 Eberle et al. Feb 1997 A
5615675 O'Donnell et al. Apr 1997 A
5660180 Malinowski et al. Aug 1997 A
5675674 Weis Oct 1997 A
5680489 Kersey Oct 1997 A
5682897 Pomeranz Nov 1997 A
5684297 Tardy et al. Nov 1997 A
5691999 Ball et al. Nov 1997 A
5693043 Kittrell et al. Dec 1997 A
5700236 Sauer et al. Dec 1997 A
5704361 Seward et al. Jan 1998 A
5718226 Riza Feb 1998 A
5732046 O'Donnell et al. Mar 1998 A
5748564 Pattanayak May 1998 A
5774610 O'rourke et al. Jun 1998 A
5779643 Lum et al. Jul 1998 A
5779644 Eberle et al. Jul 1998 A
5805332 Gopinath Sep 1998 A
5830145 Tenhoff Nov 1998 A
5844927 Kringlebotn Dec 1998 A
5852233 Arnold et al. Dec 1998 A
5857974 Eberle et al. Jan 1999 A
5865178 Yock Feb 1999 A
5872879 Hamm Feb 1999 A
5873835 Hastings et al. Feb 1999 A
5876344 Baker et al. Mar 1999 A
5894531 Alcoz Apr 1999 A
5921931 O'Donnell et al. Jul 1999 A
5938609 Pomeranz Aug 1999 A
5938615 Eberle et al. Aug 1999 A
5944687 Benett et al. Aug 1999 A
5953477 Wach et al. Sep 1999 A
5980117 Feuer et al. Nov 1999 A
6039701 Sliwa et al. Mar 2000 A
6049958 Eberle et al. Apr 2000 A
6057927 Levesque et al. May 2000 A
6078831 Belef et al. Jun 2000 A
6080109 Baker et al. Jun 2000 A
6100969 Perez Aug 2000 A
6111645 Tearney et al. Aug 2000 A
6123673 Eberle et al. Sep 2000 A
6134003 Tearney et al. Oct 2000 A
6210339 Kiepen et al. Apr 2001 B1
6218661 Schroeder et al. Apr 2001 B1
6222970 Wach et al. Apr 2001 B1
6228078 Eggers et al. May 2001 B1
6238347 Nix et al. May 2001 B1
6248076 White et al. Jun 2001 B1
6261246 Pantages et al. Jul 2001 B1
6282011 Tearney et al. Aug 2001 B1
6283920 Eberle et al. Sep 2001 B1
6292610 O'Rourke et al. Sep 2001 B1
6306096 Seward et al. Oct 2001 B1
6315732 Suorsa et al. Nov 2001 B1
6330383 Cai et al. Dec 2001 B1
6379325 Benett et al. Apr 2002 B1
6416234 Wach et al. Jul 2002 B1
6421164 Tearney et al. Jul 2002 B2
6494836 Ogawa Dec 2002 B2
6538807 Kakui et al. Mar 2003 B2
6546169 Lin et al. Apr 2003 B1
6575965 Benett et al. Jun 2003 B1
6585660 Dorando et al. Jul 2003 B2
6611633 Vohra et al. Aug 2003 B1
6618916 Eberle et al. Sep 2003 B1
6659957 Vardi et al. Dec 2003 B1
6779257 Kiepen et al. Aug 2004 B2
6783494 Ogawa Aug 2004 B2
6819845 Lee et al. Nov 2004 B2
6839496 Mills et al. Jan 2005 B1
6907163 Lewis Jun 2005 B2
6938474 Melvås Sep 2005 B2
6948859 Anderson Sep 2005 B2
6984819 Ogawa Jan 2006 B2
7082238 Nishimura Jul 2006 B2
7097620 Corl et al. Aug 2006 B2
7184148 Alphonse Feb 2007 B2
7190464 Alphonse Mar 2007 B2
7242480 Alphonse Jul 2007 B2
7242832 Carlin et al. Jul 2007 B2
7245789 Bates et al. Jul 2007 B2
7417740 Alphonse et al. Aug 2008 B2
7447388 Bates et al. Nov 2008 B2
7527594 Vardi et al. May 2009 B2
7599588 Eberle et al. Oct 2009 B2
7660492 Bates et al. Feb 2010 B2
7753852 Maschke Jul 2010 B2
7881573 Eberle et al. Feb 2011 B2
8059923 Bates et al. Nov 2011 B2
8218927 Chang et al. Jul 2012 B2
8320723 Eberle et al. Nov 2012 B2
8391652 Bates et al. Mar 2013 B2
8560048 Eberle et al. Oct 2013 B2
8731340 Bates et al. May 2014 B2
8861908 Eberle et al. Oct 2014 B2
8926519 Vardi et al. Jan 2015 B2
8968376 Wells et al. Mar 2015 B2
9078561 Eberle et al. Jul 2015 B2
9192307 Bates et al. Nov 2015 B2
9198581 Eberle et al. Dec 2015 B2
9339192 Bates et al. May 2016 B2
20010021843 Bosselmann et al. Sep 2001 A1
20010043772 Sorin Nov 2001 A1
20010046352 Ohta et al. Nov 2001 A1
20020039463 Degertekin et al. Apr 2002 A1
20020041735 Cai et al. Apr 2002 A1
20020059827 Smith May 2002 A1
20020166955 Ogawa Nov 2002 A1
20030026546 Deliwala Feb 2003 A1
20030053774 Blomquist et al. Mar 2003 A1
20030060707 Ogawa Mar 2003 A1
20030118297 Dunphy et al. Jun 2003 A1
20030181802 Ogawa Sep 2003 A1
20030187369 Lewis et al. Oct 2003 A1
20040005125 Anderson Jan 2004 A1
20040067000 Bates et al. Apr 2004 A1
20040116800 Helfer et al. Jun 2004 A1
20040182315 Laflamme, Jr. et al. Sep 2004 A1
20050020926 Wiklof et al. Jan 2005 A1
20050121734 Degertekin et al. Jun 2005 A1
20050131289 Aharoni et al. Jun 2005 A1
20050238292 Barnes et al. Oct 2005 A1
20060067616 Kanji et al. Mar 2006 A1
20070116408 Eberle et al. May 2007 A1
20070123776 Aharoni et al. May 2007 A1
20070133925 Bates et al. Jun 2007 A1
20070291275 Diamond Dec 2007 A1
20080077225 Carlin et al. Mar 2008 A1
20080114254 Matcovitch et al. May 2008 A1
20080119739 Vardi et al. May 2008 A1
20090059727 Bates et al. Mar 2009 A1
20100014810 Eberle et al. Jan 2010 A1
20100087732 Eberle et al. Apr 2010 A1
20100135111 Bates et al. Jun 2010 A1
20110123154 Eberle et al. May 2011 A1
20120108943 Bates et al. May 2012 A1
20130148933 Eberle et al. Jun 2013 A1
20130178729 Bates et al. Jul 2013 A1
20140142414 Eberle et al. May 2014 A1
20140180031 Anderson Jun 2014 A1
20140180034 Hoseit et al. Jun 2014 A1
20140200438 Millett et al. Jul 2014 A1
20140254975 Bates et al. Sep 2014 A1
20150045645 Eberle et al. Feb 2015 A1
20150313472 Eberle et al. Nov 2015 A1
20160007860 Bates Jan 2016 A1
20160097904 Eberle et al. Apr 2016 A1
Foreign Referenced Citations (52)
Number Date Country
2472877 Jul 2003 CA
2363984 Jun 1975 DE
0478410 Apr 1992 EP
1059878 Dec 2000 EP
1152240 Nov 2001 EP
2270159 Mar 1994 GB
59-158699 Sep 1984 JP
63-54151 Mar 1988 JP
02-503279 Oct 1990 JP
04-355415 Dec 1992 JP
05-015536 Jan 1993 JP
05-034550 Feb 1993 JP
05-220152 Aug 1993 JP
06-003550 Jan 1994 JP
08-112289 May 1996 JP
09-010215 Jan 1997 JP
09-187513 Jul 1997 JP
10-073742 Mar 1998 JP
63-102421 May 1998 JP
10-505920 Jun 1998 JP
10-507036 Jul 1998 JP
10-510364 Oct 1998 JP
11-194280 Jul 1999 JP
11-243596 Sep 1999 JP
11-514432 Dec 1999 JP
2000-508939 Jul 2000 JP
2001-091785 Apr 2001 JP
2002-514455 May 2002 JP
2003-232964 Aug 2003 JP
2004-085756 Mar 2004 JP
2004-177549 Jun 2004 JP
2005-079177 Mar 2005 JP
4733982 Jul 2011 JP
5445736 Jan 2014 JP
WO-8809150 Jan 1988 WO
WO-8907419 Aug 1989 WO
WO-9739691 Oct 1997 WO
WO-9958059 Nov 1999 WO
WO-0049938 Aug 2000 WO
WO-0121244 Mar 2001 WO
WO-0219898 Mar 2002 WO
WO-02054948 Jul 2002 WO
WO-02075404 Sep 2002 WO
WO-03057061 Jul 2003 WO
WO-2004008070 Jan 2004 WO
WO-2004029667 Apr 2004 WO
WO-2004032746 Apr 2004 WO
WO-2004077100 Sep 2004 WO
WO-2004090484 Oct 2004 WO
WO-2007062050 May 2007 WO
WO-2007062050 May 2007 WO
WO-2010039950 Apr 2010 WO
Non-Patent Literature Citations (225)
Entry
“U.S. Appl. No. 11/285,499, Advisory Action mailed Jun. 24, 2008”, 4 pgs.
“U.S. Appl. No. 11/285,499, Decision on Pre-Appeal Brief Request mailed Sep. 9, 2008”, 2 pgs.
“U.S. Appl. No. 11/285,499, Pre-Appeal Brief Request filed Jul. 24. 2008”, 5 pgs.
“U.S. Appl. No. 11/285,499, Response filed Feb. 15, 2007 to Restriction Requirement mailed Jan. 26, 2007”, 12 pgs.
“U.S. Appl. No. 11/285,499, Restriction Requirement mailed Jan. 26, 2007”, 4 pgs.
“U.S. Appl. No. 13/017,354, Notice of Allowance mailed Jul. 24 2012”, 7 pgs.
“U.S. Appl. No. 13/017,354, Response filed Jul. 5, 2012 to Non Final Office Action mailed Jan. 9, 2012”, 15 pgs.
“U.S. Appl. No. 14/053,421, Notice of Allowance mailed Nov. 24, 2014”, 7 pgs.
“U.S. Appl. No. 14/053,421, Response filed Sep. 22, 2014 to Non Final Office Action mailed Jun. 20, 2014”, 15 pgs.
“U.S. Appl. No. 14/280,327, Notice of Allowance mailed Jan. 27, 2015”, 7 pgs.
“U.S. Appl. No. 14/490,464, Preliminary Amendment filed Sep. 19, 2014”, 6 pgs.
“Canadian Application Serial No. 2,501,048, Office Action mailed Jun. 4, 2012”, 3 pgs.
“Canadian Application Serial No. 2,501,048, Office Action mailed Jul. 8, 2014”, 2 pgs.
“Canadian Application Serial No. 2,501,048, Office Action mailed Aug. 26, 2013”, 2 pgs.
“Canadian Application Serial No. 2,501,048, Office Action mailed Nov. 29, 2011”, 3 pgs.
“Canadian Application Serial No. 2,501,048, Response filed Feb. 11, 2014 to Office Action mailed Aug. 26, 2013”, 10 pgs.
“Canadian Application Serial No. 2,501,048, Response filed May 8, 2012 to Office Action mailed Nov. 29, 2011”, 11 pgs.
“Canadian Application Serial No. 2,501,048, Response filed Dec. 4, 2012 to Office Action mailed Jun. 4, 2012”, 17 pgs.
“Canadian Application Serial No. 2,630,662, Office Action mailed Mar. 17, 2015”, 4 pgs.
“European Application Serial No. 03756904.3 Office Action mailed Nov. 3, 2009”, 2 pgs.
“European Application Serial No. 03756904.3, Office Action mailed May 31, 2013”. 2 pgs.
“European Application Serial No. 03756904.3, Office Action mailed Aug. 1, 2011”, 4 pgs.
“European Application Serial No. 03756904.3, Response filed Feb. 13, 2012 to Office Action mailed Aug. 1, 2011”, 17 pgs.
“European Application Serial No. 03756904.3, Response filed May 13, 2010 to Office Action mailed Nov. 3, 2009”, 23 pgs.
“European Application Serial No. 03756904.3, Response filed Oct. 10, 2013 to Office Action mailed May 31, 2013”, 17 pgs.
“European Application Serial No. 06838195.3, Office Action mailed Dec. 7, 2012”, 7 pgs.
“European Application Serial No. 06838195.3, Response filed Jan. 15, 2013 to Office Action mailed Dec. 7, 2012”, 1 pg.
“European Application Serial No. 09793238.8, Amendment Filed Apr. 29, 2011”, 19 pgs.
“International Application Serial No. PCT/US2009/059218, International Preliminary Report on Patentability mailed Apr. 5, 2011”, 9 pgs.
“International Application Serial No. PCT/US2009/059218, International Search Report mailed Feb. 12, 2010”, 3 pgs.
“International Application Serial No. PCT/US2009/059218, Written Opinion mailed Apr. 2, 2011”, 8 pgs.
“Japanese Application Serial No. 2004-543092, Response filed Nov. 15, 2010 to Office Action mailed Jul. 13, 2010”, w/ English Translation of Claims), 24 pgs.
“Japanese Application Serial No. 2004-543092, Office Action mailed Jul. 13, 2010”, w/ English Translation), 3 pgs.
“Japanese Application Serial No. 2004-543092, Office Action mailed Nov. 17, 2009”, (w/ English Translation), 8 pgs.
“Japanese Application Serial No. 2004-543092, Response filed May 17, 2010 to Office Action mailed Nov. 17, 2009”, 18 pgs.
“Japanese Application Serial No. 2008-541424, Office Action mailed Oct. 30, 2012”, (w/ English Translation), 8 pgs.
“Japanese Application Serial No. 2008-541424, Response filed Jan. 29, 2013 to Office Action mailed Oct. 30, 2012”, (w/ English Translation of Amended Claims), 15 pgs.
“Japanese Application Serial No. 2010-113577, Amendment filed Nov. 15, 2010”, (w/ English Translation of Claims), 16 pgs.
“Japanese Application Serial No. 2010-113577, Office Action mailed Feb. 14, 2012”, (w/ English Translation), 4 pgs.
“Japanese Application Serial No. 2010-113577, Office Action mailed Aug. 14, 2012”, (w/ English Translation), 6 pgs.
“Japanese Application Serial No. 2010-113577, Response filed Feb. 14, 2013 to Office Action mailed Aug. 14, 2012”, 8 pgs.
“Japanese Application Serial No. 2010-113577, Response filed May 2, 2012 to Office Action mailed Feb. 14, 2012”, (w/ English Translation of Claims), 9 pgs.
“Japanese Application Serial No. 2004-543092, Notice of Allowance mailed Apr. 5, 2011”, (w/ English Translation), 2 pgs.
Optical Review, vol. 4 ,No. 6, (1997), 1 pg.
Bates, K. N., “A High Acuity 3D Acoustic Imaging System”, Proceedings., 1995 IEEE Ultrasonics Symposium, 2, (Nov. 7-10, 1995), 1245-1250.
U.S. Appl. No. 14/053,421, Notice of Allowance mailed Mar. 11, 2015, 5 pgs.
U.S. Appl. No. 14/490,464, Notice of Allowance mailed Mar. 17, 2015, 12 pgs.
“U.S. Appl. No. 09/623,248, Corrected Notice of Allowance mailed Jul. 11, 2003”, 8 pgs.
“U.S. Appl. No. 09/623,248, Examiner Interview Summary filed Nov. 6, 2003”, 1 pg.
“U.S. Appl. No. 09/623,248, Notice of Allowance mailed Jan. 13, 2003”, 7 pgs.
“U.S. Appl. No. 09/623,248, Notice of Allowance mailed Jun. 2, 2003”, 7 pgs.
“U.S. Appl. No. 09/623,248, Request for Continued Examination filed Apr. 14, 2003”, 6 pgs.
“U.S. Appl. No. 09/623,248, Supplemental Notice of Allowability mailed Oct. 7, 2003”, 6 pgs.
“U.S. Appl. No. 10/266,082, Non Final Office Action mailed Oct. 4, 2005”, 5 pgs.
“U.S. Appl. No. 10/266,082, Non-Final Office Action mailed Apr. 5, 2006”, 7 pgs.
“U.S. Appl. No. 10/266,082, Notice of Allowance mailed Jan. 12, 2005”, 5 pgs.
“U.S. Appl. No. 10/266,082, Notice of Allowance mailed Jan. 16, 2007”, 5 pgs.
“U.S. Appl. No. 10/266,082, Notice of Allowance mailed Mar. 22, 2007”, 5 pgs.
“U.S. Appl. No. 10/266,082, Notice of Allowance mailed Aug. 26, 2004”, 8 pgs.
“U.S. Appl. No. 10/266,082, Notice of Allowance mailed Sep. 22, 2006”, 4 pgs.
“U.S. Appl. No. 10/266,082, Response filed Jan. 3, 2006 to Non Final Office Action mailed Oct. 4, 2005”, 10 pgs.
“U.S. Appl. No. 10/266,082, Response filed Jul. 5, 2006 to Non Final Office Action mailed Apr. 5, 2006”, 9 pgs.
“U.S. Appl. No. 10/266,082, Response filed Jul. 28, 2004 to Restriction Requirement Jun. 29, 2004”, 2 pgs.
“U.S. Appl. No. 10/266,082, Restriction Requirement mailed Jun. 29, 2004”, 5 pgs.
“U.S. Appl. No. 10/685,226, Advisory Action mailed Apr. 17, 2006”, 3 pgs.
“U.S. Appl. No. 10/685,226, Final Office Action mailed Jan. 13, 2006”, 6 pgs.
“U.S. Appl. No. 10/685,226, Non Final Office Action mailed Jan. 18, 2007”, 6 pgs.
“U.S. Appl. No. 10/685,226, Non Final Office Action mailed Jun. 15, 2005”, 4 pgs.
“U.S. Appl. No. 10/685,226, Non Final Office Action mailed Jul. 24, 2006”, 7 pgs.
“U.S. Appl. No. 10/685,226, Notice of Allowance mailed Oct. 18, 2007”, 5 pgs.
“U.S. Appl. No. 10/685,226, Preliminary Amendment filed Oct. 14, 2003”, 1 pg.
“U.S. Appl. No. 10/685,226, Response filed Mar. 13, 2006 to Final Office Action mailed Jan. 13, 2006”, 12 pgs.
“U.S. Appl. No. 10/685,226, Response filed Apr. 18, 2007 to Non-Final Office Action mailed Jan. 18, 2007”, 10 pgs.
“U.S. Appl. No. 10/685,226, Response filed Oct. 14, 2005 to Non Final Office Action mailed Jun. 15, 2005”, 15 pgs.
“U.S. Appl. No. 10/685,226, Response filed Oct. 23, 2006 to Non Final Office Action mailed Jul. 24, 2006”, 9 pgs.
“U.S. Appl. No. 11/285,499, Examiner Interview Summary mailed May 18, 2009”, 4 pgs.
“U.S. Appl. No. 11/285,499, Final Office Action mailed Jan. 25, 2008”, 7 pgs.
“U.S. Appl. No. 11/285,499, Non Final Office Action mailed May 16, 2007”, 13 pgs.
“U.S. Appl. No. 11/285,499, Non-Final Office Action mailed Nov. 13, 2008”, 7 pgs.
“U.S. Appl. No. 11/285,499, Notice of Allowance mailed May 27, 2009”, 6 pgs.
“U.S. Appl. No. 11/285,499, Response filed Apr. 13, 2009 to Non Final Office Action mailed Nov. 13, 2008”, 14 pgs.
“U.S. Appl. No. 11/285,499, Response filed May 27, 2008 to Final Office Action mailed Jan. 25, 2008”, 9 pgs.
“U.S. Appl. No. 11/285,499, Response filed Oct. 16, 2007 to Non-Final Office Action mailed May 16, 2007”, 11 pgs.
“U.S. Appl. No. 11/674,568, Non-Final Office Action mailed Jan. 7, 2008”, 6 pgs.
“U.S. Appl. No. 11/674,568, Notice of Allowance mailed Jun. 25, 2008”, 4 pgs.
“U.S. Appl. No. 11/674,568, Response filed Apr. 21, 2008 to Non Final Office Action mailed Jan. 7, 2008”, 7 pgs.
“U.S. Appl. No. 11/674,568, Response filed Oct. 16, 2007 to Restriction Requirement mailed Sep. 17, 2007”, 7 pgs.
“U.S. Appl. No. 11/674,568, Restriction Requirement mailed Sep. 17, 2007”, 6 pgs.
“U.S. Appl. No. 12/020,736, Advisory Action mailed Feb. 13, 2014”, 3 pgs.
“U.S. Appl. No. 12/020,736, Examiner Interview Summary mailed May 8, 2014”, 3 pgs.
“U.S. Appl. No. 12/020,736, Final Office Action mailed Oct. 12, 2012”, 15 pgs.
“U.S. Appl. No. 12/020,736, Final Office Action mailed Oct. 25, 2013”, 17 pgs.
“U.S. Appl. No. 12/020,736, Non Final Office Action mailed Jun. 4, 2013”, 16 pgs.
“U.S. Appl. No. 12/020,736, Non Final Office Action mailed Sep. 30, 2011”, 12 pgs.
“U.S. Appl. No. 12/020,736, Non Final Office Action mailed Dec. 10, 2010”, 10 pgs.
“U.S. Appl. No. 12/020,736, Notice of Allowance mailed Aug. 29, 2014”, 9 pgs.
“U.S. Appl. No. 12/020,736, Response filed Mar. 13, 2014 to Advisory Action mailed Feb. 13, 2014”, 14 pgs.
“U.S. Appl. No. 12/020,736, Response filed Mar. 30, 2012 to Non Final Office Action mailed Sep. 30, 2011”, 17 pgs.
“U.S. Appl. No. 12/020,736, Response filed Apr. 12, 2013 to Final Office Action mailed Oct. 12, 2012”, 17 pgs.
“U.S. Appl. No. 12/020,736, Response filed Jun. 10, 2011 to Non-Final Office Action mailed Dec. 10, 2010”, 9 pgs.
“U.S. Appl. No. 12/020,736, Response filed Oct. 4, 2013 to Non Final Office Action mailed Jun. 4, 2013”, 18 pgs.
“U.S. Appl. No. 12/020,736, Response filed Dec. 18, 2013 to Final Office Action mailed Oct. 25, 2013”, 11 pgs.
“U.S. Appl. No. 12/020,736, Supplemental Response filed May 16, 2014 to Final Office Action mailed Oct. 25, 2013”, 13 pgs.
“U.S. Appl. No. 12/263,978, Notice of Allowance mailed Sep. 22, 2009”, 6 pgs.
“U.S. Appl. No. 12/571,724, Examiner Interview Summary mailed May 22, 2013”, 3 pgs.
“U.S. Appl. No. 12/571,724, Final Office Action mailed Jan. 4, 2013”, 13 pgs.
“U.S. Appl. No. 12/571,724, Non Final Office Action mailed Apr. 18, 2012”, 11 pgs.
“U.S. Appl. No. 12/571,724, Notice of Allowance mailed Jun. 11, 2013”, 6 pgs.
“U.S. Appl. No. 12/571,724, Response filed Jun. 4, 2013 to Final Office Action mailed Jan. 4, 2013”, 13 pgs.
“U.S. Appl. No. 12/571,724, Response filed Oct. 16, 2012 to Non Final Office Action mailed Apr. 18, 2012”, 12 pgs.
“U.S. Appl. No. 12/572,511, Non-Final Office Action mailed Jun. 1, 2010”, 8 pgs.
“U.S. Appl. No. 12/572,511, Notice of Allowance mailed Sep. 23, 2010”, 6 pgs.
“U.S. Appl. No. 12/572,511, Response filed May 17, 2010 to Restriction Requirement mailed May 10, 2010”, 7 pgs.
“U.S. Appl. No. 12/572,511, Response filed Sep. 1, 2010 to Non Final Office Action mailed Jun. 1, 2010”, 9 pgs.
“U.S. Appl. No. 12/572,511, Restriction Requirement mailed May 10, 2010”, 5 pgs.
“U.S. Appl. No. 12/701,228, Notice of Allowance mailed Apr. 22, 2011”, 8 pgs.
“U.S. Appl. No. 12/701,228, Notice of Allowance mailed Jun. 27, 2011”, 5 pgs.
“U.S. Appl. No. 13/017,354, Non Final Office Action mailed Jan. 9, 2012”, 8 pgs.
“U.S. Appl. No. 13/017,354, Non Final Office Action mailed Jun. 24, 2011”, 8 pgs.
“U.S. Appl. No. 13/017,354, Response filed Sep. 26, 2011 to Non-Final Office Action mailed Jun. 24, 2011”, 16 pgs.
“U.S. Appl. No. 13/285,551, Non Final Office Action mailed Apr. 12, 2012”, 5 pgs.
“U.S. Appl. No. 13/285,551, Notice of Allowance mailed Nov. 5, 2012”, 7 pgs.
“U.S. Appl. No. 13/285,551, Response filed Oct. 12, 2012 to Non Final Office Action mailed Apr. 12, 2012”, 8 pgs.
“U.S. Appl. No. 13/685,048, Non Final Office Action mailed Aug. 29, 2013”, 8 pgs.
“U.S. Appl. No. 13/685,048, Notice of Allowance mailed Feb. 20, 2014”, 8 pgs.
“U.S. Appl. No. 13/685,048, Notice of Allowance mailed Jun. 9, 2014”, 9 pgs.
“U.S. Appl. No. 13/685,048, Notice of Allowance mailed Nov. 22, 2013”, 10 pgs.
“U.S. Appl. No. 13/685,048, Response filed Nov. 6, 2013 to Non Final Office Action mailed Aug. 29, 2013”, 11 pgs.
“U.S. Appl. No. 13/779,985, Non Final Office Action mailed Apr. 25, 2013”, 7 pgs.
“U.S. Appl. No. 13/779,985, Notice of Allowance mailed Jan. 9, 2014”, 16 pgs.
“U.S. Appl. No. 13/779,985, Response filed Sep. 25, 2013 to Non Final Office Action mailed Apr. 25, 2013”, 12 pgs.
“U.S. Appl. No. 14/053,421, Non Final Office Action mailed Jun. 20, 2014”, 13 pgs.
“U.S. Appl. No. 14/280,327, Preliminary Amendment field Jun. 6, 2014”, 6 pgs.
“Canadian Application Serial No. 2,348,580, Office Action mailed Feb. 20, 2007”, 2 pgs.
“Canadian Application Serial No. 2,348,580, Response filed Aug. 16, 2007 to Office Action mailed Feb. 20, 2007”, 7 pgs.
“Canadian Application Serial No. 2,630,662, Office Action mailed Sep. 6, 2013”, 3 pgs.
“Canadian Application Serial No. 2,630,662, Response filed Mar. 6, 2014 to Office Action mailed Sep. 6, 2013”, 15 pgs.
“European Application Serial No. 05024287.4, Examination Notification Art. 94(3) mailed Apr. 25, 2014”, 4 pgs.
“European Application Serial No. 05024287.4, Office Action mailed Feb. 9, 2012”, 4 pgs.
“European Application Serial No. 05024287.4, Office Action mailed Sep. 22, 2006”, 1 pg.
“European Application Serial No. 05024287.4, Office Action mailed Sep. 25, 2012”, 1 pg.
“European Application Serial No. 05024287.4, Response filed Nov. 23, 2012 to Office Action mailed Sep. 25, 2012”, 9 pgs.
“European Application Serial No. 05024287.4, Response filed Jun. 6, 2007 to Office Action mailed Sep. 22, 2006”, 8 pgs.
“European Application Serial No. 05024287.4, Search Report mailed Jan. 3, 2006”, 7 pgs.
“European Application Serial No. 06838195.3, Office Action mailed Jul. 27, 2009”, 4 pgs.
“European Application Serial No. 06838195.3, Response filed Feb. 4, 2010 to Office Action mailed Jul. 27, 2009”, 8 pgs.
“European Application Serial No. 99950325.3, Amendment filed Feb. 7, 2005”, 11 pgs.
“European Application Serial No. 99950325.3, European Search Report mailed Mar. 8, 2004”, 3 pgs.
“European Application Serial No. 99950325.3, Office Action mailed Jul. 28, 2004”, 3 pgs.
“International Application Serial No. PCT/US03/31280, Demand and Response filed May 6, 2004 to Partial Search Report mailed Dec. 2, 2004”, 13 pgs.
“International Application Serial No. PCT/US03/31280, International Preliminary Examination Report mailed Feb. 1, 2005”, 16 pgs.
“International Application Serial. No. PCT/US03/31280, International Search Report mailed Jul. 19, 2004”, 5 pgs.
“International Application Serial. No. PCT/US03/31280, Invitation to Pay Additional Fees and Partial Search Report mailed Feb. 12, 2004”, 10 pgs.
“International Application Serial No. PCT/US2003/031280, Response filed Jan. 19, 2005 to Written Opinion mailed Jan. 14, 2005”, 14 pgs.
“International Application Serial No. PCT/US2003/031280, Written Opinion mailed Jan. 14, 2005”, 7 pgs.
“International Application Serial No. PCT/US2006/045080, International Preliminary Report on Patentability mailed Jun. 5, 2008”, 10 pgs.
“International Application Serial No. PCT/US2006/045080, International Search Report and Written Opinion mailed May 16, 2007”, 16 pgs.
“International Application Serial No. PCT/US2006/045080, Invitation to Pay Additional Fees and Partial International Search Report mailed Mar. 9, 2007”, 4 pgs.
“International Application Serial No. PCT/US2006/045080, Partial International Search Report mailed Mar. 9, 2007”, 3 pgs.
“International Application Serial No. PCT/US99/04913, International Search Report mailed May 28, 1999”, 1 pg.
“Japanese Application Serial No. 2000-547913, Office Action mailed Feb. 24, 2009”, w/ English translation, 7 pgs.
“Japanese Application Serial No. 2000-547913, Office Action mailed Jun. 23, 2009”, w/ English translation, 8 pgs.
“Japanese Application Serial No. 2000-547913, Response filed May 22, 2009 to Office Action mailed Feb. 24, 2009”, w/ English Translaion of Claims, 9 pgs.
“Japanese Application Serial No. 2000-547913, Response filed Dec. 18, 2009 to Office Action mailed Jun. 23, 2009”, w/ English Translation of Claims, 12 pgs.
“Japanese Application Serial No. 2008-541424, Amendment filed Nov. 16, 2009”, w/ English Translation of Claims, 10 pgs.
“Japanese Application Serial No. 2008-541424, Office Action mailed Sep. 3, 2013”, w/ English Translation, 6 pgs.
“Japanese Application Serial No. 2008-541424, Response filed Oct. 29, 2013 to Office Action mailed Sep. 13, 2013”, w/ English claims, 9 pgs.
“Tissue Characterization through Ultrasonic Backscatter”, [Online]. Retrieved from the Internet: <URL: http://www.brl.uiuc.edu/Projects/backscatter.htm>, (retrieved Sep. 25, 2002), 5 pgs.
Bates, K. N., “A One Dimensional Phased Array Imaging System”, Ph.D. Dissertation, Applied Physics, Stanford University, (1982), 186 pgs.
Bates, K. N., et al., “PEOATS and ESOATS”, IEEE Ultrasonics Symposium Proceedings, 1979, (Sep. 26-28, 1979), 189-194.
Bates, K. N., “Tolerance Analysis for Phased Arrays”, Acoustic Imaging, 9, (1980), 239-262.
Bates, Kenneth N, “A high acuity 3-D acoustic imaging system”, Proceedings., 1995 IEEE Ultrasonics Symposium, 2, (Nov. 7-10, 1995), 1245-1250.
Bates, Kenneth N., et al., “Digitally Controlled Electronically Scanned and Focused Ultrasonic Imaging System”, IEEE Ultrasonics Symposium Proceedings, 1979, (Sep. 26-28, 1979), 216-220.
Blotekjaer, K., “Theoretical concepts of a novel Vernier-based fringe-counting fibre optic sensor”, IEE Proceedings, Optoelectronics, 144(3), (Jun. 1997), 126-129.
Brady, G. P, et al., “Simultaneous measurement of strain and temperature using the first- and second-order diffraction wavelengths of Bragg gratings”, IEE Proceedings, and Optoelectronics, 144(3), (Jun. 1997), 156-161.
Buma, T., et al., “A high frequency ultrasound array element using thermoelastic expansion in PDMS”, Proceedings of the 2001 IEEE Ultrasonics Symposium, 2, (Oct. 7-10, 2001), 1143-1146.
Buma, T., et al., “A high-frequency, 2-D array element using thermoelastic expansion in PDMS”, IEEE Transactions on Ultrasonics, Ferroelectrics and Frequency Control, 50(9), (Sep. 2003), 1161-1176.
Buma, T., et al., “High Frequency Ultrasonic Imaging Using Optoacoustic Arrays”, Proceedings of the Proceeding of the 2002 IEEE Ultrasonics Symposium, 1, Invited paper, (Oct. 8-11, 2002), 571-580.
Buma, T., et al., “High Frequency Ultrasound Array Element using Thermoelastic Expansion in an Elastomeric Film”, Applied Physics Letters, 79(4), (Jul. 23, 2001), 548-550.
Buma, T., et al., “High-frequency ultrasound imaging using opto-acoustic arrays”, Proceedings of the SPIE—The International Society for Optical Engineering, 4687, (2002), 99-109.
Buma, T., et al., “Thermoelastic Expansion versus Piezoelectricity for High Frequency 2-D Arrays”, IEEE Transactions on Ultrasonics, Ferroelectrics and Frequency Control, 50(8), (Aug. 2003), 1065-1068.
Buma, T., et al., “Thermoelastic Generation of Continuous Lamb Waves for Microfluidic Devices”, Proceeding of the 2003 IEEE Ultrasonics Symposium, (2003), 150-153.
Buma, T., et al., “Thermoelastic Generation of Ultrasound Using anErbium Doped Fiber Amplifier”, Proceeding of the 1999 IEEE Ultrasonics Symposium, 2, (Oct. 17-20, 1999), 1253-1256.
Davis, M. A, et al., “Simultaneous measurement of temperature and strain using fibre Bragg gratings and Brillouin scattering”, IEE Proceedings, Optoelectronics, 144(3), (Jun. 1997), 151-155.
Feced, R., et al., “Advances in high resolution distributed temperature sensing using the time-correlated single photon counting technique”, IEE Proceedings, Optoelectronics, 144(3), (Jun. 1997), 183-188.
Furstenau, N., et al., “Extrinsic Fabry-Perot interferometer vibration and acoustic sensor systems for airport ground traffic monitoring”, IEE Proceedings, Optoelectronics, 144(3), (Jun. 1997), 134-144.
Hamilton, J. D., et al., “An active optical detector for high frequency ultrasound imaging”, Proceedings of the 1997 IEEE Ultrasonics Symposium, 1, (Oct. 5-8, 1997), 753-756.
Hamilton, J. D., et al., “High frequency optoacoustic arrays using etalon detection”, IEEE Transactions on Ultrasonics, Ferroelectrics and Frequency Control, 47(1), (Jan. 2000), 160-169.
Hamilton, J. D., et al., “High Frequency Ultrasound Imaging Using an Active optical Detector”, IEEE Transactions on Ultrasonics, Ferroelectrics and Frequency Control UFFC-45, (1998), 719-727.
Hamilton, J. D., et al., “High Frequency Ultrasound Imaging with Optical Arrays”, IEEE Transactions on Ultrasonics, Ferroelectrics and Frequency Control, 45(1), (Jan. 1998), 216-235.
Hamilton, J. D., et al., “Optical Arrays for High Frequency Ultrasound Imaging”, Proceedings of the 1996 IEEE Ultrasonics Symposium, (1996), 1419-1422.
Karl, W Clem, “Multi-Sensor Fusion for Atherosclerotic Plaque Characterization”, Boston University—MDSP, [online] Retrieved from the internet:<http://www.censsis.neu/Education/Student Research/2001/posters/weisensell)rl.pdf>, (Retrieved Sep. 25, 2002), 15 pgs.
Komiyama, N., et al., “Tissue Characterization of Atherosclerotic Plaques by Intravascular Ultrasound Radiofrequency Signal Analysis: An In Vitro Study of Human Coronary Arteries” American Heart Journal, 140(4) (Oct. 2000), 565-574.
Krass, S., et al., “P3.4 Pattern Recognition Algorithms for Tissue Characterization in Intracoronary Ultrasound Imaging: Test Data Set and Results of Computerized Texture Analysis”, 2nd Medical Clinic, Univ-Mainz, Germany, [online]. Retrieved from the Internet: <URL: http://www.uni-mainz.de/Cardio/incis/Data/p3—4.htm>, (Accessed on Sep. 25, 2002), 3 pgs.
Lockey, R. A, et al., “Multicomponent time-division-multiplexed optical fibre laser Doppler anemometry”, IEE Proceedings, Optoelectronics, 144(3), (Jun. 1997), 168-175.
Macpherson, W. N, et al., “Phase demodulation in optical fibre Fabry-Perot sensors with inexact phase steps”, IEE Proceedings, Optoelectronics, 1440, (Jun. 1997), 130-133.
McCulloch, S., et al., “Development of a fibre optic micro-optrode for intracellular pH measurements”, IEE Proceedings, Optoelectronics, 1440, (Jun. 1997), 162-167.
Mintz, Gary S., et al., “American College of Cardiology Clinical Expert Consensus Document on Standards for Acquisition, Measurement and Reporting of Intravascular Ultrasound Studies (IVUS)”, Journal of the American College of Cardiology, 37(5), (Apr. 2001), 1478-1492.
Moreira, P J, et al., “Dynamic Range Enhancement in Fiber Bragg Grating Sensors using a Multimode Laser Diode”, IEEE Photonics Technology Letters, vol. 11, No. 6, (Jun. 1999), 3 pgs.
O'Donnell, M., “New Imaging Technologies for Ultrasonography”, J Med Ultrason., 27(4), Presented at the 73rd Japan Society of Ultrasound in Medicine Meeting, Invited Paper, (2000), 356-357.
O'Donnell, M., et al., “Optoacoustics: high frequency ultrasonic array imaging”, Proceedings of 17th International Congress on Acoustics, vol. IV, Biomedicine, Acoustics in Medicine, Invited Presentation at the 17th Intl Congress on Acoustics, Rome, (Sep. 2-7, 2001), 2-3.
Othonos, A., et al., “In Section 7.9 Bragg Gating Fiber Laser Sensors from Fiber Bragg Gratings: fundamentals and applications in telecommunications and sensing”, Artech House, Inc., (1999), 355-367.
Pepine, Carl J., et al., “Improving Diagnostic and Therapeutic Outcomes Through Advanced Intravascular Imaging”, Vascular Technologies, Inc., (1989), 3 pgs.
Scully, P. J., “UV Laser Photo-induced Refractive Index Changes in Poly-Methyl-Meth Acrylate and Plastic Optical Fibres for Application as Sensors and Devices”, Central Laser Facility Annual Report, 1999/2000, (1999-2000), 145-147.
Siebes, M., et al., “Single-Wire Pressure and Flow Velocity Measurement to Quantify Coronary Stenosis Hemodynamics and Effects of Percutaneous Interventions”, Circulation, 109, (2004), 756-762.
Spisar, M., et al., “Stabilized, Resonant Optoacoustic Array Detectors for Medical Imaging”, Proceedings of the World Congress on Ultrasonics, Paris, France, (Sep. 7-10, 2003), 25-28.
Stefanadis, Christodoulos, et al., “Identification and Stabilization of Vulnerable Atherosclerotic Plaques: The Role of Coronary Thermagraphy and External Heat Delivery”, [online]. Retrieved from the Internet:<URL:http://www.indianheartjournal.org/Jan-Feb-2001/identification/indentification/htm>, (2001), 10 pgs.
Surowiec, J., et al., “A Novel Miniature Optical Fibre Probe for MHz Frequency Ultrasound”, Proceedings, IEEE Ultrasonics Symposium, vol. 2, (Nov. 3-6, 1996, San Antonio, TX), (1996), 1051-1054.
Takahashi, N., et al., “Underwater Acoustic Sensor with Fiber Bragg Grating”, Optical Review, 4(6), (1997), 691-694.
Tanaka, S., et al., “Fibre optic spectral polarimetry for sensing multiple stress-loaded locations along a length of fibre”, IEE Proceedings, Optoelectronics, 144(3), (Jun. 1997), 176-182.
Wahle, Andreas, et al., “Accurate Visualization and Quantification of Coronary Vasculature by 3-D/4-D Fusion from Biplane Angiography and Intravascular Ultrasound”, In: Biomonitoring and Endoscopy Technologies; I. Gannot et al., eds, (Jul. 5-6, 2000), 144-155.
Yoshino, T., et al., “Spiral fibre microbend sensors”, IEE Proceedings, Optoelectronics,144(3), (Jun. 1997), 145-150.
“U.S. Appl. No. 14/280,327, Notice of Allowance mailed May 22, 2015”, 5 pgs.
“U.S. Appl. No. 14/490,464, Notice of Allowance mailed Aug. 4, 2015”, 9 pgs.
“U.S. Appl. No. 14/796,767, Non Final Office Action mailed Sep. 29, 2015”, 9 pgs.
“U.S. Appl. No. 14/796,767, Preliminary Amendment filed Jul. 14, 2015”, 6 pgs.
“U.S. Appl. No. 14/796,767, Response filed Dec. 17, 2015 to Non-Final Office Action mailed Sep. 29, 2015”, 8 pgs.
“U.S. Appl. No. 14/836,705, Preliminary Amendment filed Sep. 30, 2015”, 5 pgs.
“U.S. Appl. No. 14/952,690, Preliminary Amendment filed Dec. 16, 2015”, 6 pgs.
“U.S. Appl. No. 14/836,705, Notice of Allowance mailed Jan. 12, 2016”, 8 pgs.
“Canadian Application Serial No. 2,501,048, Office Action mailed Feb. 9, 2016”, 3 pgs.
“Canadian Application Serial No. 2,501,048, Office Action mailed May 15, 2015”, 3 pgs
“Canadian Application Serial No. 2,501,048, Response filed Nov. 2, 2015 to Office Action mailed May 15, 2015”, 10 pgs.
“Canadian Application Serial No. 2,630,662, Response filed Sep. 1, 2015 to Office Action mailed Mar. 17, 2015”, 18 pgs.
U.S. Appl. No. 14/952,690, Non Final Office Action mailed May 12, 2016, 21 pgs.
Related Publications (1)
Number Date Country
20150190113 A1 Jul 2015 US
Provisional Applications (1)
Number Date Country
60076862 Mar 1998 US
Continuations (3)
Number Date Country
Parent 12020736 Jan 2008 US
Child 14577980 US
Parent 10685226 Oct 2003 US
Child 12020736 US
Parent 09623248 US
Child 10685226 US