FDA applicant

Arvee Medical, Inc.

Battle Creek, MI3 decisions1987–19900 recalls

FDA records 3 decisions for Arvee Medical, Inc. (Battle Creek, MI) from 1987 to 1990: 3 510(k) clearances. All are in product code BZQ (Monitor, Breathing Frequency). 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, anesthesiology panel, where it files most

How often FDA has decided Arvee Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Arvee Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Arvee Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?