# Pancretec, Inc.

- Location (FDA's records): San Diego, CA
- FDA decisions: 10 (1984–1988): 10 510(k) clearances
- Product codes: FRN (7), FPA (3)
- 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
- K882102: Provider One Infusion System (Aug 12, 1988)
- K871806: Provider IV. Model 5000 Infusion Device (Oct 22, 1987)
- K844078: Provider PA 3000 Infusion System (Dec 18, 1984)
- K843463: Provider Bag Spike W/12 Microbore Exten (Oct 11, 1984)
- K841373: Provider IV Model 2000 Infusin Sys (May 14, 1984)
- K841017: Provider Infusion Set (Apr 30, 1984)
- K841027: Provider Site Prep & Check Strip Kit (Apr 16, 1984)
- K833983: Provider U-100 Insulin Infusion Sys (Apr 13, 1984)

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