FDA applicant

Autonomic Equipment Supply Co,

Mchenry, IL2 decisions1978–19810 recalls

FDA records 2 decisions for Autonomic Equipment Supply Co, (Mchenry, IL) from 1978 to 1981: 2 510(k) clearances. All are in product code KNM (Device, Pressure 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 Autonomic Equipment Supply Co,’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Autonomic Equipment Supply Co, since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Autonomic Equipment Supply Co, by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Autonomic Equipment Supply Co,

Which product codes does it file in?

What has FDA decided for it lately?