510(k) K251258 · DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
MC2 Two-Stage Venous Cannula; MC2X Three-Stage Venous Cannula
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Jun 20, 2025 |
| Received | Apr 23, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251258
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.