510(k) K890077 ยท DTN Reservoir, Blood, Cardiopulmonary Bypass
TRAUMAFUSE RAPID INFUSION DEVICE
| Applicant | The Traumafuse Co., Allentown PA, US |
| Decision | Substantially Equivalent, Apr 3, 1989 |
| Received | Jan 9, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890077
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.