510(k) K894255 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
ST.JUDE MEDICAL PULSE 2100 CENTRIFUGAL PUMP
| Applicant | St. Jude Medical, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Sep 26, 1989 |
| Received | Jun 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894255
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.