# Omnimedical

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1979–1983): 6 510(k) clearances
- Product codes: JAK (3), IZL (1), FMH (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
- K837378: Omnimedical Quad II Digital Angiograph System (May 18, 1983)
- K820180: Calculi Filter Cup (Feb 5, 1982)
- K812393: 4001 CT Scanner (Oct 13, 1981)
- K812400: Omnimedical Quad I (Oct 2, 1981)
- K802206: Omni Scanner CT 6000 (Oct 23, 1980)
- K790673: Omnimedical Automatic 1001 (May 4, 1979)

Source page: https://510kreport.com/company/omnimedical