# Khi, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1980–1983): 4 510(k) clearances
- Product codes: BTL (2), CAI (1), BTC (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
- K830404: Rad Valve (Mar 17, 1983)
- K830399: Coupling/Valve (Mar 10, 1983)
- K811858: Khi Cpram Breathing Circuit (Jul 16, 1981)
- K800456: Emergiency Resuscitator/Inhalor W/Aspir. (Mar 18, 1980)

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