510(k) K140165 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
MC2 TWO-STAGE VENOUS CANNULA, OVAL MC2 TWO-STAGE VENOUS CANNULA, THIN WALL TWO-STAGE VENOUS CANNULA, MC2X THREE-STAGE VE
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, May 20, 2014 |
| Received | Jan 22, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140165
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.