# Preco, Inc.

- Location (FDA's records): Oakland, NJ
- FDA decisions: 4 (1985–1985): 4 510(k) clearances
- Product codes: JHJ (1), DHR (1), GMQ (1), KTN (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
- K853144: Card Three IM Test Item #2035, Card One IM #2036 (Oct 16, 1985)
- K852751: Tolvidine Red Unheated Serum Syphillis Card Test (Aug 20, 1985)
- K853054: RF Card Test (Aug 1, 1985)
- K850604: Preco Pregnancy Rapid Card Test, Hem #2028 (Apr 8, 1985)

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