FDA applicant

Nor-Am Patient Care Products, Inc.

Walker, MI7 decisions1985–19900 recalls

FDA records 7 decisions for Nor-Am Patient Care Products, Inc. (Walker, MI) from 1985 to 1990: 7 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and IMI (Ultrasonic Diathermy For Use In Applying…). 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, physical medicine panel, where it files most

How often FDA has decided Nor-Am Patient Care Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nor-Am Patient Care Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nor-Am Patient Care Products, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Nor-Am Patient Care Products, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?