510(k) K040173 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
PEDIATRIC AORTIC ROOT CANNULA
| Applicant | Medtronic Perfusion Systems, Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 19, 2004 |
| Received | Jan 26, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K040173
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.