Cardiovascular Devices, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K890113 | THE CDI(R) SYSTEM 400 | May 23, 1989 |
| K884228 | CDI(R) 2000 BLOOD GAS MONITOR | January 30, 1989 |
| K871221 | CDI(TM) EXTRACORPOREAL BLOOD GAS SYSTEM 300 | June 5, 1987 |
| K864703 | MODIFIED GAS-STAT(TM) MONITORING SYSTEM | February 19, 1987 |
| K843912 | INTRAVASCULAR BLOOD GAS SYSTEM | January 10, 1985 |
| K840749 | GAST STAT MONITORING SYSTEM | April 17, 1984 |
| K831225 | GAS-STAT MONITORING SYSTEM | May 27, 1983 |
| K822000 | EXTRACORPOREAL BLOOD GAS SYSTEM | December 22, 1982 |