510(k) Report

FDA applicant

General Medical Co.

Mchenry, IL15 decisions1977–19930 recalls

FDA records 15 decisions for General Medical Co. (Mchenry, IL) from 1977 to 1993: 15 510(k) clearances. Most are in product codes EGJ (Device, Iontophoresis, Other Uses) and FRG (Wrap, Sterilization). 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 General Medical Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for General Medical Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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