# Gynopharma, Inc.

- Location (FDA's records): Princeton, NJ
- FDA decisions: 2 (1991–1991): 2 510(k) clearances
- Product codes: HFF (1), HIT (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
- K903001: Slimcath (TM) (Jun 25, 1991)
- K903002: Probet (TM) (Apr 5, 1991)

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