510(k) K052372 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C
| Applicant | Medtronic Perfusion Systems, Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 22, 2005 |
| Received | Aug 30, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K052372
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.