510(k) Report

FDA applicant

American Hamilton

Mchenry, IL3 decisions1981–19820 recalls

FDA records 3 decisions for American Hamilton (Mchenry, IL) from 1981 to 1982: 3 510(k) clearances. Most are in product codes GDC (Table, Operating-Room, Electrical) and FNM (Mattress, Air Flotation, Alternating Pressure). 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 and plastic surgery panel, where it files most

How often FDA has decided American Hamilton’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Hamilton since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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