# Avi, Inc.

- Location (FDA's records): St. Paul, MN
- FDA decisions: 13 (1981–1988): 13 510(k) clearances
- Product codes: FRN (13)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 32 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K882047: Entrust (TM) Model 800 (Aug 11, 1988)
- K875348: Model 400A Infusion Pump (Apr 29, 1988)
- K875347: Model 210A Infusion Pump (Apr 29, 1988)
- K875365: Model 200A Infusion Pump (Apr 29, 1988)
- K872516: Infusion Pump Model 275 (Dec 16, 1987)
- K872514: Infusion Pump Model 270 (Dec 16, 1987)
- K872515: Infusion Pump Model 470 (Dec 16, 1987)
- K854073: Model 210 Infusion Pump (Dec 10, 1985)

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