Life-Tech Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Life-Tech Instruments, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Life-Tech Instruments, Inc. has 19 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1977 to 1981. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Life-Tech Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Life-Tech Instruments, Inc.
19 devices
Cleared
Sep 09, 1981
LIFE-TECH #1857 PRESSURE/POLOT MODULE
Gastroenterology & Urology
37d
Cleared
Aug 25, 1981
LIFE-TECH #1753 BIOFEEDBACK TRAINER
Neurology
22d
Cleared
Aug 21, 1981
LIFE-TECH #5102 VISULAB
Neurology
18d
Cleared
Aug 13, 1981
LIFE-TECH #'S 1106/1156 UROLABS
Gastroenterology & Urology
10d
Cleared
Mar 10, 1980
AMBLYOPIA TRAINER
Ophthalmic
54d
Cleared
Apr 24, 1979
MODEL 1750 STANDING URINAL
Gastroenterology & Urology
18d
Cleared
Apr 23, 1979
MODEL 1309 AUDIO MONITOR
Neurology
17d
Cleared
Nov 15, 1978
MULAR GOLD LEAF ELECTRODE MODEL 7501
Ophthalmic
79d
Cleared
Nov 08, 1978
MODEL 7320 VISUAL STIMULATOR
Neurology
82d
Cleared
Sep 07, 1978
PREAMPLIFIER MODELS 8101PI & 8102PI
Ear, Nose, Throat
10d
Cleared
Sep 07, 1978
ELECTRODE IMPEDANCE TESTER-MODEL 500
Neurology
10d
Cleared
Jun 22, 1978
STIMULATOR MODEL 8021
Neurology
80d
Cleared
Jun 02, 1978
EAR ELECTRODE-ADULT & PEDIATRIC
Neurology
60d
Cleared
May 19, 1978
PRESSURE MODULES MODELS 1855 & 1856
Neurology
46d
Cleared
Apr 21, 1978
ELECTRIC RESPONSE AUDIOMETER
Neurology
18d
Cleared
Apr 19, 1978
AUDIO MONITOR-MODEL 8309
Neurology
16d
Cleared
Jun 03, 1977
URODYNAMIC INSTRUMENTS
Gastroenterology & Urology
18d
Cleared
May 23, 1977
CATHETER, URETHRAL PRESSURE, UPE-10 & 12
Gastroenterology & Urology
56d
Cleared
Feb 28, 1977
SYS. FOR REC. BSER RESPONSES
Neurology
17d