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Life-Tech Intl., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
68
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K001129PROLONG, MODELS PL50, PL100, PL150July 6, 2000
K954505EZ STIMDecember 10, 1996
K955031MAXISTIMDecember 10, 1996
K954315PVC ABDOMINAL/RECTAL PRESSURE CATHETERNovember 30, 1995
K954341URODYNAMICS TUBING AND INFUSION SETSOctober 17, 1995
K953451UROPUMP TUBE & DAMPING CHAMGEROctober 5, 1995
K953353UROVISION JANUSSeptember 8, 1995
K946108EAR-A-GATORJune 13, 1995
K913601MICROPHORJuly 15, 1994
K940203TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERSMarch 30, 1994
K931179UROLAB SPECTRUMNovember 18, 1993
K931282VOLUME TRANSDUCERSeptember 17, 1993
K923612MODIFIED F-10 CULTURE MEDIUM W/O HYPOXANTHINESeptember 7, 1993
K923651DISTILLED WATERSeptember 7, 1993
K923634MODIFIED F-10 CULTURE MEDIUMSeptember 7, 1993
K923652DULBECCO'S PHOSPHATE BUFFERED SALINESeptember 7, 1993
K926349PROBLOC INSULATED NEEDLESJuly 29, 1993
K923072HANDTYMPMarch 18, 1993
K923073AUTOMATIC TYMPANOMETERFebruary 19, 1993
K923071DANPLEX DIAGNOSTIC AUDIOMETER, CLIN. DIAG. AUDIOMTSeptember 28, 1992