FDA applicant

3M Avi, Inc.

St. Paul, MN18 decisions1990–19930 recalls

FDA records 18 decisions for 3M Avi, Inc. (St. Paul, MN) from 1990 to 1993: 18 510(k) clearances. Most are in product codes FRN (Pump, Infusion) and FPA (Set, Administration, Intravascular). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided 3M Avi, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for 3M Avi, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — 3M Avi, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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3M Avi, Inc.

Which product codes does it file in?

What has FDA decided for it lately?