510(k) K001371 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CARDEON ASCENDING BALLOON CANNULA (ABC)
| Applicant | Cardeon Corp., Cupertino CA, US |
| Decision | Substantially Equivalent, Jul 7, 2000 |
| Received | May 1, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001371
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.