510(k) K253203 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Retrograde Coronary Sinus Perfusion Cannulae
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, Feb 19, 2026 |
| Received | Sep 26, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K253203
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.