510(k) K042156 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CARDEON COBRA CATHETER
| Applicant | Cardeon Corp., Cupertino CA, US |
| Decision | Substantially Equivalent, Oct 6, 2004 |
| Received | Aug 10, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042156
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.