510(k) K133151 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
SARNS HIGH FLOW AORTIC ARCH CANNULA
| Applicant | Terumo Cardiovascular Systems Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Feb 3, 2014 |
| Received | Oct 17, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133151
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.