# Cardiovascular Devices, Inc.

- Location (FDA's records): Irvine, CA
- FDA decisions: 8 (1982–1989): 8 510(k) clearances
- Product codes: DTY (3), DRY (2), CBZ (1), DJY (1), CCE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- 3M Company: 1 (https://510kreport.com/company/3m)
- 3M Healthcare: 1 (https://510kreport.com/company/3m-healthcare)

## Its most-cited devices
- K890113: The Cdi (R) System 400 (1989), cited by 2

## Recent decisions
- K890113: The Cdi (R) System 400 (May 23, 1989)
- K884228: Cdi (R) 2000 Blood Gas Monitor (Jan 30, 1989)
- K871221: Cdi (TM) Extracorporeal Blood Gas System 300 (Jun 5, 1987)
- K864703: Modified Gas-Stat (TM) Monitoring System (Feb 19, 1987)
- K843912: Intravascular Blood Gas System (Jan 10, 1985)
- K840749: Gast Stat Monitoring System (Apr 17, 1984)
- K831225: Gas-Stat Monitoring System (May 27, 1983)
- K822000: Extracorporeal Blood Gas System (Dec 22, 1982)

Source page: https://510kreport.com/company/cardiovascular-devices