Life-Tech Intl., Inc. - FDA 510(k) Cleared Devices
68
Total
66
Cleared
0
Denied
Life-Tech Intl., Inc. has 66 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 66 cleared submissions from 1982 to 2000. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Life-Tech Intl., Inc. Filter by specialty or product code using the sidebar.
68 devices
Cleared
Jul 06, 2000
PROLONG, MODELS PL50, PL100, PL150
Anesthesiology
90d
Cleared
Dec 10, 1996
EZ STIM
Anesthesiology
439d
Cleared
Dec 10, 1996
MAXISTIM
Anesthesiology
404d
Cleared
Nov 30, 1995
PVC ABDOMINAL/RECTAL PRESSURE CATHETER
Gastroenterology & Urology
76d
Cleared
Oct 17, 1995
URODYNAMICS TUBING AND INFUSION SETS
Gastroenterology & Urology
29d
Cleared
Oct 05, 1995
UROPUMP TUBE & DAMPING CHAMGER
Gastroenterology & Urology
79d
Cleared
Sep 08, 1995
UROVISION JANUS
Gastroenterology & Urology
53d
Cleared
Jun 13, 1995
EAR-A-GATOR
Ear, Nose, Throat
181d
Cleared
Jul 15, 1994
MICROPHOR
Physical Medicine
1067d
Cleared
Mar 30, 1994
TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS
Gastroenterology & Urology
76d
Cleared
Nov 18, 1993
UROLAB SPECTRUM
Gastroenterology & Urology
254d
Cleared
Sep 17, 1993
VOLUME TRANSDUCER
Gastroenterology & Urology
189d
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