510(k) K921550 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
LIFESTREAM CENTRIFUGAL PUMP SYSTEM MODEL 2100CP
| Applicant | St. Jude Medical, Inc., Chelmsford MA, US |
| Decision | Substantially Equivalent, May 21, 1992 |
| Received | Mar 24, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921550
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.