510(k) K061254 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
EOPA 3D ARTERIAL CANNULA, MODELS 78220,78222,78320,783222
| Applicant | Medtronic Perfusion Systems, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jun 23, 2006 |
| Received | May 4, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K061254
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.