510(k) K902404 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
SARNS DELPHIN CENTRIFUGAL SYSTEM W/DIRECTION. FLOW
| Applicant | 3M Company, Ann Arbor MI, US |
| Decision | Substantially Equivalent, Dec 17, 1990 |
| Received | May 30, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902404
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.