TREA

Applicator

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Information

  • Patent Grant
  • D1036656
  • Patent Number
    D1,036,656
  • Date Filed
    Wednesday, September 16, 2020
    3 years ago
  • Date Issued
    Tuesday, July 23, 2024
    a month ago
  • US Classifications
    Field of Search
    • US
    • D24 108
    • D24 112
    • D24 113
    • D24 114
    • D24 115
    • D24 127-131
    • D24 133
    • D24 186
    • D24 216
    • D24 224
    • D24 111
    • D24 119
    • D24 137
    • D24 138
    • D24 141
    • D24 147
    • D24 177
    • D24 214
    • D24 222
    • D09 418
    • D09 434
    • D09 435
    • D09 447
    • D09 448
    • D09 449
    • D09 452
    • D09 453
    • D09 454
    • D09 724
    • D28 7
    • D23 233-250
    • D23 207
    • D23 209
    • D23 365
    • CPC
    • A61M25/00
    • A61M39/00
    • A61M27/00
    • A61M25/0043
    • A61M25/0067
    • A61M25/0097
    • A61F2/958
    • B01D35/143
    • B01D2201/304
    • B01D27/10
    • B01D27/106
    • A61K31/12
    • A61K31/365
    • A61K36/29
    • A61K31/7048
    • A61K31/60
  • International Classifications
    • 2402
    • Term of Grant
      15Years
Information
Abstract
Description


FIG. 1 is a perspective view of an applicator;



FIG. 2 is a right side view thereof, the left side view being a mirror image to the right side view;



FIG. 3 is a top view thereof; and,



FIG. 4 is a bottom view thereof.


The surface shading shown in FIGS. 1-2 indicates that the claimed applicator is transparent. Material, texture, color, surface finish and surface ornamentation form no part of the claimed design.


The dot-dash-dot lines represent the bounds of the claimed design that form no part of the claimed design. The remaining broken lines illustrate portions of the applicator that form no part of the claimed design.


Claims
  • The ornamental design for an applicator, as shown and described.
US Referenced Citations (75)
Number Name Date Kind
1744893 Hein Jan 1930 A
3393962 Maurice Jul 1968 A
3981924 Hall Sep 1976 A
4148874 Smith Apr 1979 A
4157967 Meyst et al. Jun 1979 A
4299006 Cruz Nov 1981 A
4413154 Dessau Nov 1983 A
5445462 Johnson et al. Aug 1995 A
5464855 Capiris et al. Nov 1995 A
5590780 O'Meara Jan 1997 A
5702694 Chamness Dec 1997 A
6066124 Caillouette May 2000 A
D436661 Berry Jan 2001 S
6379342 Levinson Apr 2002 B1
6547467 Quintero Apr 2003 B2
6673031 Mark Jan 2004 B2
6811342 Pauchet Nov 2004 B2
8518076 Stenton Aug 2013 B2
8871801 Levitt Oct 2014 B2
D771250 Zhang et al. Nov 2016 S
D772407 Zhang et al. Nov 2016 S
9480691 Roth Nov 2016 B1
D801830 Zhang et al. Nov 2017 S
10195635 Sporrer Feb 2019 B2
D868160 Lam Nov 2019 S
10745413 Davidson et al. Aug 2020 B2
D900312 Davidson Oct 2020 S
11052064 Davidson Jul 2021 B2
D933494 Tempfli Oct 2021 S
11147790 Welgus et al. Oct 2021 B2
11168091 Davidson et al. Nov 2021 B2
D938587 Fujii Dec 2021 S
D947027 Marik Mar 2022 S
11279165 Skinner Mar 2022 B2
D957625 Reynolds Jul 2022 S
D969312 Daniel Nov 2022 S
11559294 Pollack Jan 2023 B2
20030068331 Battaglia et al. Apr 2003 A1
20040152766 Au-Yeung et al. Aug 2004 A1
20040254561 Stenton Dec 2004 A1
20050019418 Crutchfield et al. Jan 2005 A1
20050111900 Fazzolari et al. May 2005 A1
20050169696 Albisetti Aug 2005 A1
20060110415 Gupta May 2006 A1
20060116649 Hagele Jun 2006 A1
20060180613 Manesis Aug 2006 A1
20070000566 Gueret Jan 2007 A1
20070111954 Crutchfield et al. May 2007 A1
20070187437 Lord Aug 2007 A1
20070233020 Hearne Oct 2007 A1
20070233021 Poisson et al. Oct 2007 A1
20070275045 Evans et al. Nov 2007 A1
20080146674 Rosenberg et al. Jun 2008 A1
20080195040 Clark et al. Aug 2008 A1
20090311028 Odermatt et al. Dec 2009 A1
20110208136 Sollingen et al. Aug 2011 A1
20110212033 Tamarkin et al. Sep 2011 A1
20120016320 Lin Jan 2012 A1
20120148520 Strobel et al. Jun 2012 A1
20120190658 Studin Jul 2012 A1
20120312709 Kaufman Dec 2012 A1
20130004230 Kirk et al. Jan 2013 A1
20130197075 Levitt Aug 2013 A1
20140275248 Johnson Sep 2014 A1
20150118164 Tamarkin et al. Apr 2015 A1
20150328259 Shanler et al. Nov 2015 A1
20160193177 Davidson Jul 2016 A1
20170305925 Piotrowski et al. Oct 2017 A1
20190002474 Davidson et al. Jan 2019 A1
20190031674 Davidson et al. Jan 2019 A1
20200155498 Welgus et al. May 2020 A1
20200270269 Davidson et al. Aug 2020 A1
20210138214 Davidson et al. May 2021 A1
20210386703 Davidson Dec 2021 A1
20210401793 Welgus et al. Dec 2021 A1
Foreign Referenced Citations (48)
Number Date Country
204207 Apr 1939 CH
1571795 Jan 2005 CN
101012230 Aug 2007 CN
101108853 Jan 2008 CN
101108854 Jan 2008 CN
101161654 Apr 2008 CN
101798309 Aug 2010 CN
102146086 Aug 2011 CN
102268006 Dec 2011 CN
102336765 Feb 2012 CN
102526146 Jul 2012 CN
202730045 Feb 2013 CN
202920809 May 2013 CN
103923095 Jul 2014 CN
204817029 Dec 2015 CN
105636637 Jun 2016 CN
106674248 May 2017 CN
20016131 Nov 2000 DE
0841059 May 1998 EP
587994 May 1947 GB
S51-141863 Dec 1976 JP
05-058914 Mar 1993 JP
H05-255367 Oct 1993 JP
10-114626 May 1998 JP
11-319064 Nov 1999 JP
11-335303 Dec 1999 JP
2004-059446 Feb 2004 JP
2005-187330 Jul 2005 JP
2007-269693 Oct 2007 JP
2008-505960 Feb 2008 JP
2010-516410 May 2010 JP
2010-235471 Oct 2010 JP
47-39621 Aug 2011 JP
2013-507367 Mar 2013 JP
2016-528015 Sep 2016 JP
2017-513907 Jun 2017 JP
10-2005-0032154 Apr 2005 KR
10-2016-0045086 Apr 2016 KR
10-2017-0029413 Mar 2017 KR
WO 2008092068 Jul 2008 WO
WO 2010002476 Jan 2010 WO
2012131238 Oct 2012 WO
WO 2013189841 Dec 2013 WO
2015027111 Feb 2015 WO
WO 2016006693 Jan 2016 WO
2016100732 Jun 2016 WO
WO 2016118633 Jul 2016 WO
2018226894 Dec 2018 WO
Non-Patent Literature Citations (69)
Entry
Extended European Search Report, mailed Mar. 10, 2017, in connection with EP 14837297.2.
International Search Report and Written Opinion, mailed Nov. 20, 2014, in connection with PCT/US2014/052184.
Extended European Search Report, mailed Oct. 26, 2018, in connection with EP 15871116.8.
Supplementary European Search Report, mailed Aug. 8, 2018, in connection with EP 16740681.8.
Extended European Search Report, mailed Dec. 4, 2018, in connection with EP 16740681.8.
Invitation to Pay Additional Fees, mailed Aug. 27, 2018, in connection with PCT/US2018/O3653.
International Search Report and Written Opinion, mailed Oct. 22, 2018, in connection with PCT/US2018/036353.
Invitation to Pay Additional Fees, mailed Sep. 20, 2018, in connection with PCT/US2018/037808.
International Search Report and Written Opinion, mailed Nov. 13, 2018, in connection with PCT/US2018/037808.
International Preliminary Report on Patentability mailed Dec. 26, 2019 in connection with International Application No. PCT/US2018/037808.
Invitation to Pay Additional Fees, mailed Dec. 10, 2018, in connection with PCT/US2018/054373.
International Search Report and Written Opinion, mailed Apr. 3, 2019 in connection with PCT/US2018/054373.
International Preliminary Report on Patentability mailed Apr. 16, 2020, in connection with International Application No. PCT/US2018/054373.
[No Author Listed] CAS RN 27607-77-8. Entered STN: Nov. 16, 1984. 28 pages.
[No Author Listed] CAS RN 76262-87-8. Entered STN: Nov. 16, 1984. 19 pages.
[No Author Listed] CAS RN 89672-77-5. Entered STN: Nov. 16, 1984. 29 pages.
Aitken et al., Fragmentation patterns in the gas-phase pyrolysis of some bi- and tri-cyclic sulfolanes related to the 8-thiabicyclo[4.3.0]non-3-ene 8,8-dioxide ring system . J Chem Soc. Perkin Transactions 1. 1994;16:2301-2308.
Anderson et al., Practical Process Research and Development. 1st Edition. Academic Press. Mar. 20, 2000. 81-111.
Augé et al., Catalysis by Lithium Cation: Lithium Trifluoromethanesulfonate as a Substitute for Lithium Perchlorate in Cycloadditions. Synlett 2000;6:877-9.
Bouacha et al., A theoretical study of the mechanism, stereoselectivity and Lewis acid catalyst on the Diels-Alder cycloaddition between furan and activated alkenes. Tetrahedron Letters. 2013;54:4030-4033.
Braddock et al., Stereochemistry of the Catalysed Diels-Alder Reaction between Cyclopentadiene and Dimethyl Monothionofumarate; Soft versus Hard Lewis Acids. J. Chem. Soc. Chem. Commun. Jan. 1, 1993;16:1244-6. doi: https://doi.org/10.1039/C39930001244.
Brion et al., On the lewis acid catalyzed diels-alder reaction of furan. regio- and stereospecific synthesis of substituted cyclohexenols and cyclohexadienols. Tetrahedron Letters. 1982;23(50):5299-302. https://doi.org/10.1016/S0040-4039(00)85823-2.
Hollis et al., Homogeneous catalysis. Titanium complex [Ti(Cp)2(CF3SO3)2] and zirconium complex [Zr(Cp)2(CF3SO3)2THF], efficient catalysts for the Diels-Alder reaction. Organometallics. Aug. 1, 1992;11(8):2745-8. https://doi.org/10.1021/om00044a004.
Hollis et al., Homogenous Catalysis: Transition Metal Based Lewis Acid Catalysts. Tetrahedron. 1993;49(25):5415-30. doi: https://doi.org/10.1016/S0040-4020(01)87259-8.
Houk et al., On Lewis Acid catalysis of diels-alder reactions. J Am Chem Soc. Jun. 13, 1973;95(12):4094-4096.
Huang, Catalysts for Hetero Diels-Alder Reaction of Imines. Chinese Journal of Organic Chemistry. Oct. 2003;23(10):1064-75.
Hubbard et al., Lewis Acid Catalyzed Diels?Alder Reactions of Highly Hindered Dienophiles. J. Org. Chem. 1998;63(12):4143-4146.
Hunt et al., Why do catalytic quantities of lewis acid generally yield more product than 1.1 equiv in the intramolecular diels-adler reaction with a furan diene? Competitive complexation NMR studies provide an answer. J Am Chem Soc. 1995;117:1049-1056.
Kharitonov et al., Synthetic transformations of higher terpenoids: VIII. [4+2]-Cycloaddition reactions of lambertianic acid. Russian J Organic Chem. 2003;39(1):57-74.
Lange et al., Synthesis of 4-carboxy-2-thiabicyclo [3.2.0] Heptan-6-ones via 3-carboxy-2,3-dihydrothiophenes: potential ?-lactamase inhibitors. Tetrahedron Lett. 1985;26(15):1791-1794.
Pagni et al., A chemical, spectroscopic, and theoretical assessment of the lewis acidity of LiClO4 in Diethyl Ether. J. Org Chem. 1993;58:3130-3133.
Prabhakar Reddy et al., Synthesis, cytotoxic activity and structure-activity relationships of hedychenone analogues. Bioorg Med Chem Lett. Apr. 15, 2010;20(8):2525-8. doi: 10.1016/j.bmcl.2010.02.101. Epub Mar. 3, 2010.
Song et al., Ionic liquids as powerful media in scandium triflate catalysed Diels-Alder reactions: significant rate acceleration, selectivity improvement and easy recycling of catalyst. Chem Commun. 2001;12:1122-3.
Sperry et al., Studies on the Diels-Alder reaction of annulated furans: application to the synthesis of substituted phenanthrenes. Tetrahedron Letters. Apr. 18, 2005;46(16):2789-93. Doi: 10.1016/j.tetlet.2005.02.148.
Tseng et al., Synthesis and Evaluation of Cantharidinimides on Human Cancer Cells. J Exp Clin Med. Oct. 2012;4(5):280-283.
U.S. Appl. No. 14/913,335, filed Feb. 19, 2016, Davidson.
U.S. Appl. No. 15/535,860, filed Jun. 14, 2017, Davidson et al.
U.S. Appl. No. 16/995,606, filed Aug. 17, 2020, Davidson et al.
U.S. Appl. No. 15/544,669, filed Jul. 19, 2017, Davidson et al.
U.S. Appl. No. 16/619,675, filed Dec. 5, 2019, Welgus et al.
U.S. Appl. No. 16/621,854, filed Dec. 12, 2019, Davidson et al.
U.S. Appl. No. 16/753,660, filed Apr. 3, 2020, Davidson et al.
U.S. Appl. No. 29/607,744, filed Jun. 15, 2017, Davidson et al.
[No Author Listed] Journal of Organic Chemistry Author Guidelines. Last updated May 5, 2022. 3 pages.
Chen et al., Precautions with gentian violet: skin marking made sterile, effective, and economical. Am J Infect Control. Apr. 2009;37(3):244-6. doi: 10.1016/j.ajic.2008.06.005. Epub Oct. 14, 2008.
Chung et al., Sequential Nitromethane Conjugate Addition/Elimination—PD-Catalyzed Allylation of beta-Trifloxy Acrylates. Application to Carbapenem Synthesis. Org Lett. 1999;1(11):1783-1785.
Earle et al., Diels-Alder reactions in ionic liqu1449—. A safe recyclable alternative to lithium perchlorate-diethyl ether mixtures. Green Chem. Feb. 1999; 1:23-25. doi: 10.1039/A808052F.
Gaul, Part I. Diels-Alder reactions performed in highly polar media. Part II. Reactions of allenylstannanes with in situ generated immonium ions. Dissertation. Indiana University, Bloomington Indiana, 1990. 152 pages.
Harreus et al., 2-Pyrrolidone. Ullmann's Encyclopedia of Industrial Chemistry. 2000. doi: doi: 10.1002/14356007.a22_457.pub2.
Pulce et al., Denatonium Benzoate. Human Toxicol. Jan. 1996;1-12. Accessed 2022 Sep. 12 from <https://www.sciencedirect.com/topics/medicine-and-dentistry/denatonium-benzoate>.
Rossy et al., Aromatization of Dihyrothiophenes. Thiophenesaccharin: A Sweet Surprise. J Org Chem. 1980;45:617-620.
White et al., Quinoline Analogues of Ortho-Quinodimethane. Tetrahedron Lett. 1995;36(33):5983-5986.
EP 14837297.2, Date of Mailing Mar. 10, 2017, *Extended European Search Report.
PCT/US2014/052184, Date of Mailing Nov. 20, 2014, *International Search Report and Written Opinion.
EP 15871116.8, Date of Mailing Oct. 26, 2018, *Extended European Search Report.
PCT/US2015/066487, Date of Mailing Jul. 14, 2016, *International Search Report and Written Opinion.
PCT/US2015/066487, Date of Mailing Jun. 29, 2017, *International Preliminary Report on Patentability.
EP 16740681.8, Date of Mailing Aug. 8, 2018, *Supplementary European Search Report.
EP 16740681.8, Date of Mailing Dec. 4, 2018, *Extended European Search Report.
PCT/US2016/014139, Date of Mailing Jul. 1, 2016, *International Search Report and Written Opinion.
PCT/US2016/014139, Date of Mailing Aug. 3, 2017, *International Preliminary Report on Patentability.
PCT/US2018/036353, Date of Mailing Aug. 27, 2018, *Invitation to Pay Additional Fees.
PCT/US2018/036353, Date of Mailing Oct. 22, 2018, *International Search Report and Written Opinion.
PCT/US2018/037808, Date of Mailing Sep. 20, 2018, *Invitation to Pay Additional Fees.
PCT/US2018/037808, Date of Mailing Nov. 13, 2018, *International Search Report and Written Opinion.
PCT/US2018/037808, Date of Mailing Dec. 26, 2019, *International Preliminary Report on Patentability.
PCT/US2018/054373, Date of Mailing Dec. 10, 2018, *Invitation to Pay Additional Fees.
PCT/US2018/054373, Date of Mailing Apr. 3, 2019, *International Search Report and Written Opinion.
PCT/US2018/054373, Date of Mailing Apr. 16, 2020, *International Preliminary Report on Patentability.
Divisions (1)
Number Date Country
Parent 29607744 Jun 2017 US
Child 29750763 US