510(k) K263596 · DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
DLP Coronary Ostial Cannulae
| Applicant | Medtronic, Inc., Brooklyn Park MN, US |
| Decision | Substantially Equivalent, Oct 29, 2026 |
| Received | Sep 30, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K263596
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.