FDA applicant

Omnicon Medical Corp.

Mchenry, IL10 decisions1976–19830 recalls

FDA records 10 decisions for Omnicon Medical Corp. (Mchenry, IL) from 1976 to 1983: 10 510(k) clearances. Most are in product codes CAH (Filter, Bacterial, Breathing-Circuit) and CAI (Circuit, Breathing (W Connector, Adaptor, Y…). 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, anesthesiology panel, where it files most

How often FDA has decided Omnicon Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Omnicon Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Omnicon Medical Corp.

Which product codes does it file in?

What has FDA decided for it lately?