510(k) K131269 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
DLP CORONARY OSTIAL PERFUSION CANNULAE
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 10, 2013 |
| Received | May 3, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131269
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 10, 2024 | Medtronic Perfusion Systems Medtronic DLP Coronary Ostial Cannulae, Model Number 30050 Open, Classified |
DWF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.