510(k) K871221 ยท DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
CDI(TM) EXTRACORPOREAL BLOOD GAS SYSTEM 300
| Applicant | Cardiovascular Devices, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jun 5, 1987 |
| Received | Mar 27, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871221
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.