# Canyon Medical Products

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 3 (1988–1995): 3 510(k) clearances
- Product codes: DWF (2), KYX (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
- K954181: Canyons BI-Directional Check Valve (Nov 29, 1995)
- K897026: Canyon Medical Femoral Bypass Cannulae and Intro. (Feb 26, 1990)
- K874899: Canyon Medical Femoral Bypass Cannulae (Feb 18, 1988)

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