510(k) K180453 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, Mar 22, 2018 |
| Received | Feb 20, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K180453
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.