Home / Companies / Life-Tech Instruments, Inc.

Life-Tech Instruments, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K812177LIFE-TECH #1857 PRESSURE/POLOT MODULESeptember 9, 1981
K812179LIFE-TECH #1753 BIOFEEDBACK TRAINERAugust 25, 1981
K812180LIFE-TECH #5102 VISULABAugust 21, 1981
K812178LIFE-TECH #'S 1106/1156 UROLABSAugust 13, 1981
K800112AMBLYOPIA TRAINERMarch 10, 1980
K790663MODEL 1750 STANDING URINALApril 24, 1979
K790664MODEL 1309 AUDIO MONITORApril 23, 1979
K781476MULAR GOLD LEAF ELECTRODE MODEL 7501November 15, 1978
K781461MODEL 7320 VISUAL STIMULATORNovember 8, 1978
K781474PREAMPLIFIER MODELS 8101PI & 8102PISeptember 7, 1978
K781475ELECTRODE IMPEDANCE TESTER-MODEL 500September 7, 1978
K780539STIMULATOR MODEL 8021June 22, 1978
K780537EAR ELECTRODE-ADULT & PEDIATRICJune 2, 1978
K780541PRESSURE MODULES MODELS 1855 & 1856May 19, 1978
K780540ELECTRIC RESPONSE AUDIOMETERApril 21, 1978
K780538AUDIO MONITOR-MODEL 8309April 19, 1978
K770897URODYNAMIC INSTRUMENTSJune 3, 1977
K770579CATHETER, URETHRAL PRESSURE, UPE-10 & 12May 23, 1977
K770268SYS. FOR REC. BSER RESPONSESFebruary 28, 1977