# Omnicon Medical Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 10 (1976–1983): 10 510(k) clearances
- Product codes: CAH (5), CAI (2), CAE (1), EWC (1), FMP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K823872: Emergency Tracheostomy Kit (Jan 21, 1983)
- K820577: Anesthesia Bacteria Filter (Mar 18, 1982)
- K820576: Mainflow Bacteria Filter (Mar 18, 1982)
- K801803: Mainflow Bacteria Filter (Aug 13, 1980)
- K801804: Anesthesia Bacteria Filter (Aug 13, 1980)
- K772060: Protect IV Gard (Dec 20, 1977)
- K770136: Disposable Bacteria Filter (Feb 14, 1977)
- K770001: Airway, Berman 40, 60, 80, 90, L00MM'S (Jan 12, 1977)

Source page: https://510kreport.com/company/omnicon-medical