510(k) K882129 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
SYMBION CENTRIFUGAL BLOOD PUMP MODEL I
| Applicant | Symbion, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Nov 3, 1988 |
| Received | May 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882129
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.