510(k) K151523 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Uncoated Tubing and Connector Components
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 16, 2015 |
| Received | Jun 5, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151523
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.