510(k) K142673 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Bio-Medicus Adult Cannulae and Introducer
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Nov 18, 2014 |
| Received | Sep 19, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142673
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.