Home / Companies / Life-Tech Intl., Inc.

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
K923634MODIFIED F-10 CULTURE MEDIUMSeptember 7, 1993
K923652DULBECCO'S PHOSPHATE BUFFERED SALINESeptember 7, 1993
K923651DISTILLED WATERSeptember 7, 1993
K926349PROBLOC INSULATED NEEDLESJuly 29, 1993
K923072HANDTYMPMarch 18, 1993
K923073AUTOMATIC TYMPANOMETERFebruary 19, 1993
K923071DANPLEX DIAGNOSTIC AUDIOMETER, CLIN. DIAG. AUDIOMTSeptember 28, 1992