510(k) K913176 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
DELPHIN II CENTRIFUGAL SYSTEM
| Applicant | 3M Health Care, Sarns, Ann Arbor MI, US |
| Decision | Substantially Equivalent, Nov 7, 1991 |
| Received | Jul 17, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913176
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.