510(k) K952879 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
SARNS CENTRIFUGAL PUMP WITH DURAFLO II TREATMENT
| Applicant | Baxter Healthcare Corp, Irvine CA, US |
| Decision | Substantially Equivalent, Apr 22, 1996 |
| Received | Jun 23, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952879
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.