Ampcor, Inc.
Ampcor, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1992.
Top product codes for Ampcor, Inc.
Recent clearances by Ampcor, Inc.
- K922296 — IMFECTIOUS MONONUCLEOSIS IM LIQUID CARD TEST
- K922297 — INFECTIOUS MONONUCLEOSIS QIK-DOT IM DRY CARD TEST
- K910438 — DIPSTICK SALMONELLA
- K893873 — SINGLE AND DUAL BAND DIPSTICK HCG TEST
- K890048 — QUIK-DOT TOXOPLASMOSIS
- K892119 — QUIK-DOT C REACTIVE PROTEIN
- K892146 — C REACTIVE PROTEIN LIQUID
- K890025 — QUIK-DOT ANTISTREPTOLYSIN-O
- K884750 — GROUP A STREP, BETA-STREP
- K880163 — PREGNANCY (HCG) CARD & LIQUID TEST
- K880478 — PREGNANCY BETA-HCG CARD & LIQUID TEST
- K880165 — TRUST RPR TEST FOR SYPHILIS IN SERUM OR PLASMA
- K880477 — RPR TEST FOR SYPHILIS IN SERUM OR PLASMA
- K880148 — INFECTIOUS MONONUCLEOSIS (IM) CARD & LIQUID TEST
- K880164 — RF CARD TEST & RF LIQUID TEST
Data sourced from openFDA. This site is unofficial and independent of the FDA.