510(k) Report

FDA applicant

Med General

Mchenry, IL12 decisions1977–19791 recall

FDA records 12 decisions for Med General (Mchenry, IL) from 1977 to 1979: 12 510(k) clearances. Most are in product codes GDJ (Clamp, Surgical, General & Plastic Surgery) and GXY (Electrode, Cutaneous). 1 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 Med General’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Med General since 2007.

Recalls per year

1in 2018

2018: 1
2007high 1 (2018) · low 0 (2007)2026

Class I Class II/III not classified

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

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