510(k) K902355 ยท DTP Defoamer, Cardiopulmonary Bypass
MCR4000 & MCR4000F CARDIOTOMY RESERVOIR
| Applicant | Medtronic Vascular, Anaheim CA, US |
| Decision | Substantially Equivalent, Aug 23, 1990 |
| Received | May 29, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902355
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.