510(k) K895393 ยท DTZ Oxygenator, Cardiopulmonary Bypass
SARNS INGANT MEMBRANE OXYGENATOR
| Applicant | 3M Company, Ann Arbor MI, US |
| Decision | Substantially Equivalent, Dec 4, 1989 |
| Received | Sep 5, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895393
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.