# 3M Avi, Inc.

- Location (FDA's records): St. Paul, MN
- FDA decisions: 18 (1990–1993): 18 510(k) clearances
- Product codes: FRN (16), FPA (2)
- 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
- K912069: Avi Model 4225 Vented Piggyback IV Admin Set (Oct 14, 1993)
- K912590: Avi Model 400D Infusion Pump (Oct 17, 1991)
- K912589: Avi Model 840D Dual Channel Infusion Pump (Oct 17, 1991)
- K912591: Avi Micro 210D Infusion Pump (Sep 6, 1991)
- K912875: Avi Model 270CI Infusion Pump (Aug 20, 1991)
- K912738: Avi Volumetric Infusion Pumps-Various Models (Aug 12, 1991)
- K912031: Avi Model 870 Dual Channel Infusion Pump (Jun 18, 1991)
- K904979: Avi Model 600 Syringe Pump, Modification (Jan 15, 1991)

Source page: https://510kreport.com/company/3m-avi