510(k) K123762 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH AUTO-INFLATE CUFF
| Applicant | Medtronic, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 27, 2013 |
| Received | Dec 7, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123762
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.