# Cryosan, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 6 (1981–1983): 6 510(k) clearances
- Product codes: KZL (2), GKT (1), GIF (1), LKN (1), FIR (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
- K831953: Infusion Pump (Jul 19, 1983)
- K830831: Automated Blood Cell Separator (Jun 16, 1983)
- K822521: Automated Blood Cell Separator (Sep 30, 1982)
- K813489: Rocking/Circulating Cyto-Therm II 3570 (Mar 4, 1982)
- K812311: Circulating Cyto-Therms (Sep 16, 1981)
- K812309: Cryosan Normal Saline (Sep 16, 1981)

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