510(k) K120987 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
DLP SINGLE STAGE VENOUS CANNULA INFLATABLE CUFF
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 6, 2012 |
| Received | Apr 2, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120987
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.