510(k) K791832 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
VEIN GRAFT CANNULA
| Applicant | D/P, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 4, 1979 |
| Received | Sep 18, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791832
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.