Ampcor, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K922296IMFECTIOUS MONONUCLEOSIS IM LIQUID CARD TESTJuly 14, 1992
K922297INFECTIOUS MONONUCLEOSIS QIK-DOT IM DRY CARD TESTJuly 14, 1992
K910438DIPSTICK SALMONELLASeptember 13, 1991
K893873SINGLE AND DUAL BAND DIPSTICK HCG TESTAugust 21, 1989
K890048QUIK-DOT TOXOPLASMOSISJune 9, 1989
K892146C REACTIVE PROTEIN LIQUIDApril 14, 1989
K892119QUIK-DOT C REACTIVE PROTEINApril 14, 1989
K890025QUIK-DOT ANTISTREPTOLYSIN-OJanuary 31, 1989
K884750GROUP A STREP, BETA-STREPDecember 22, 1988
K880163PREGNANCY (HCG) CARD & LIQUID TESTMay 17, 1988
K880478PREGNANCY BETA-HCG CARD & LIQUID TESTApril 28, 1988
K880165TRUST RPR TEST FOR SYPHILIS IN SERUM OR PLASMAMarch 30, 1988
K880477RPR TEST FOR SYPHILIS IN SERUM OR PLASMAMarch 30, 1988
K880148INFECTIOUS MONONUCLEOSIS (IM) CARD & LIQUID TESTFebruary 10, 1988
K880164RF CARD TEST & RF LIQUID TESTFebruary 10, 1988