510(k) K943861 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
CAPIOX SP PUMP HEAD
| Applicant | Terumo Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Aug 15, 1995 |
| Received | Aug 8, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943861
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.