510(k) K031827 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
ULTRAFLEX VENOUS CANNULA, MODEL 970XX AND CB970XX
| Applicant | Medtronic Perfusion Systems, Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 2, 2003 |
| Received | Jun 13, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031827
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.