# Cooper Medical Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 5 (1982–1984): 5 510(k) clearances
- Product codes: HHR (1), LLF (1), HQE (1), FCG (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
- K840144: Yag Laser 8000 Gastrointestinal Blee (May 18, 1984)
- K833387: Argon Laser Surgical System 770 (Apr 18, 1984)
- K833497: Cooper Medical Model 770 (Apr 17, 1984)
- K832703: Argon Laser Sys-Model 5000 (Jan 30, 1984)
- K820261: Monitor CO2 Laser System (Mar 5, 1982)

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