510(k) K890808 ยท DTZ Oxygenator, Cardiopulmonary Bypass
SARNS MEMBRANE OXYGENATOR W/INTEGRAL CARDIO RESERV
| Applicant | 3M Company, Ann Arbor MI, US |
| Decision | Substantially Equivalent, May 1, 1989 |
| Received | Feb 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890808
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.