510(k) K140192 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CARPENTIER BI-CAVAL FEMORAL CANNULA
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, May 22, 2014 |
| Received | Jan 27, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140192
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.