FDA 510(k) Applications Submitted by Jeff Kasoff

FDA 510(k) Number Submission Date Device Name Applicant
K050499 02/28/2005 PROBLOC, HN SERIES AND PROLONG, PL SERIES LIFE-TECH, INC.
K160846 03/28/2016 AmplifEYE MEDIVATORS, INC.
K001129 04/07/2000 PROLONG, MODELS PL50, PL100, PL150 LIFE-TECH INTL., INC.
K151522 06/05/2015 DEFENDO Bronchoscopy Suction Valve MEDIVATORS, INC.
K081864 07/01/2008 PROLONG LIFE-TECH, INC.
K102007 07/16/2010 PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC, LIFE-TECH, INC.
K082056 07/21/2008 ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1 LIFE-TECH, INC.
K072050 07/26/2007 PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS LIFE-TECH, INC.
K082772 09/22/2008 STIMPRO, MODELS SP22050, SP20100, SPP19050, SPP19100, SPP19150, SPC19050, SPC19100, SPC19150, SPC18050,SPC18100,SPC18150 LIFE-TECH, INC.
K082923 10/01/2008 PRLONG, MODELS PL50, PL100, PL-40C, PL-50C, PL-100C, PL-150C, PLT-40C, PLT-50C, PLT-100C, PLT-150C LIFE-TECH, INC.
K052954 10/20/2005 CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SET LIFE-TECH, INC.
K093485 11/09/2009 VESISCAN LIFE-TECH, INC.
K073187 11/13/2007 PERIPHERAL NERVE BLOCK SUPPORT TRAY LIFE-TECH, INC.
K093662 11/25/2009 ECHOBRIGHT LIFE-TECH, INC.


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