# Diamond Medical, Inc.

- Location (FDA's records): St. Paul, MN
- FDA decisions: 6 (1987–1992): 6 510(k) clearances
- Product codes: FFT (4), CHL (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K924758: Dmi Blood Gas Analyzer/Cartridge (Dec 3, 1992)
- K915087: Dmi Blod Gas Analyzer/Cartridge (Jan 8, 1992)
- K874710: Diamond Medical, Inc. Model DM 600 (Feb 8, 1988)
- K874709: Diamond Medical, Inc. Model DM 800 (Feb 8, 1988)
- K875369: Model Iso-2001 Univ. Patient Isolation Circuit (Feb 5, 1988)
- K863298: Diamond Medical, Inc., Model DM 700 (Mar 17, 1987)

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