510(k) K972740 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
HIMEX CENTRIFLOW CENTRIFUGAL PERFUSION PUMP SYSTEM (CFK01)
| Applicant | Himex Production Corp., Houston TX, US |
| Decision | Substantially Equivalent, Feb 6, 1998 |
| Received | Jul 22, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972740
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.