Life-Tech, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Life-Tech, Inc. has 14 FDA 510(k) cleared anesthesiology devices. Based in Stafford, US.
Historical record: 14 cleared submissions from 2005 to 2012.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Apr 19, 2012
EZONO 3000
Radiology
85d
Cleared
Sep 16, 2011
ECHOBRIGHT
Anesthesiology
123d
Cleared
Jun 30, 2011
EZONO 3000
Radiology
275d
Cleared
Dec 22, 2010
PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,
Anesthesiology
159d
Cleared
Jun 24, 2010
ECHOBRIGHT
Anesthesiology
211d
Cleared
Mar 16, 2010
VESISCAN
Radiology
127d
Cleared
Feb 09, 2009
STIMPRO, MODELS SP22050, SP20100, SPP19050, SPP19100, SPP19150, SPC19050,...
Anesthesiology
140d
Cleared
Nov 07, 2008
ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1
Gastroenterology & Urology
109d
Cleared
Oct 24, 2008
PRLONG, MODELS PL50, PL100, PL-40C, PL-50C, PL-100C, PL-150C, PLT-40C,...
Anesthesiology
23d
Cleared
Sep 25, 2008
PROLONG
Anesthesiology
86d
Cleared
Apr 22, 2008
PERIPHERAL NERVE BLOCK SUPPORT TRAY
Anesthesiology
161d
Cleared
Oct 18, 2007
PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS
Anesthesiology
84d