510(k) K052524 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT
| Applicant | Medtronic Perfusion Systems, Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 22, 2005 |
| Received | Sep 14, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052524
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.