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Ampcor, Inc.

FDA 510(k) & PMA Approved Devices — 15 products

Total Devices15
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K922297 INFECTIOUS MONONUCLEOSIS QIK-DOT IM DRY CARD TESTKTN1992-07-14 View
510(k) K922296 IMFECTIOUS MONONUCLEOSIS IM LIQUID CARD TESTKTN1992-07-14 View
510(k) K910438 DIPSTICK SALMONELLAGRM1991-09-13 View
510(k) K893873 SINGLE AND DUAL BAND DIPSTICK HCG TESTDHA1989-08-21 View
510(k) K890048 QUIK-DOT TOXOPLASMOSISLLA1989-06-09 View
510(k) K892119 QUIK-DOT C REACTIVE PROTEINDCK1989-04-14 View
510(k) K892146 C REACTIVE PROTEIN LIQUIDDCK1989-04-14 View
510(k) K890025 QUIK-DOT ANTISTREPTOLYSIN-OGTQ1989-01-31 View
510(k) K884750 GROUP A STREP, BETA-STREPGTZ1988-12-22 View
510(k) K880163 PREGNANCY (HCG) CARD & LIQUID TESTJHJ1988-05-17 View
510(k) K880478 PREGNANCY BETA-HCG CARD & LIQUID TESTJHJ1988-04-28 View
510(k) K880165 TRUST RPR TEST FOR SYPHILIS IN SERUM OR PLASMAGMQ1988-03-30 View
510(k) K880477 RPR TEST FOR SYPHILIS IN SERUM OR PLASMAGMQ1988-03-30 View
510(k) K880148 INFECTIOUS MONONUCLEOSIS (IM) CARD & LIQUID TESTKTN1988-02-10 View
510(k) K880164 RF CARD TEST & RF LIQUID TESTDHR1988-02-10 View
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