510(k) K902845 ยท DWE Tubing, Pump, Cardiopulmonary Bypass
GENTLE HEADER
| Applicant | Enhanced Perfusion Systems, Inc., Grass Lake MI, US |
| Decision | Substantially Equivalent, Dec 3, 1990 |
| Received | Jun 28, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902845
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.