FDA applicant

Con Med Equipment, Inc.

Mchenry, IL3 decisions1981–19830 recalls

FDA records 3 decisions for Con Med Equipment, Inc. (Mchenry, IL) from 1981 to 1983: 3 510(k) clearances. Most are in product codes KGX (Tape And Bandage, Adhesive) and DRX (Electrode, Electrocardiograph). 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 Con Med Equipment, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Con Med Equipment, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Con Med Equipment, Inc.

Which product codes does it file in?

What has FDA decided for it lately?