510(k) K000274 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
EOPA ELONGATED ONE-PIECE ARTERIAL CANNULA WITH GUIDEWIRE
| Applicant | Medtronic Cardiac Surgical Products, Grand Rapids MI, US |
| Decision | Substantially Equivalent, Feb 10, 2000 |
| Received | Jan 31, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000274
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.