# Ampcor, Inc.

- Location (FDA's records): Bridgeport, NJ
- FDA decisions: 15 (1988–1992): 15 510(k) clearances
- Product codes: KTN (3), DCK (2), GMQ (2), JHJ (2), DHA (1), GRM (1), LLA (1), GTQ (1), DHR (1), GTZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K922296: Imfectious Mononucleosis IM Liquid Card Test (Jul 14, 1992)
- K922297: Infectious Mononucleosis Qik-Dot IM Dry Card Test (Jul 14, 1992)
- K910438: Dipstick Salmonella (Sep 13, 1991)
- K893873: Single and Dual Band Dipstick HCG Test (Aug 21, 1989)
- K890048: Quik-Dot Toxoplasmosis (Jun 9, 1989)
- K892146: C Reactive Protein Liquid (Apr 14, 1989)
- K892119: Quik-Dot C Reactive Protein (Apr 14, 1989)
- K890025: Quik-Dot Antistreptolysin-O (Jan 31, 1989)

Source page: https://510kreport.com/company/ampcor