510(k) K983791 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
PERIPHERAL RETROGRADE CARDIAPLEGIA CANNULA
| Applicant | Edwards Lifesciences Research Medical, Midvale UT, US |
| Decision | Substantially Equivalent, Jun 11, 1999 |
| Received | Oct 27, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983791
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.