510(k) K894721 ยท DWE Tubing, Pump, Cardiopulmonary Bypass
TRAUMAFUSE PERFUSION PRESSURE RELIEF VALVE
| Applicant | The Traumafuse Co., Allentown PA, US |
| Decision | Substantially Equivalent, Oct 20, 1989 |
| Received | Jul 25, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894721
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.