510(k) K863740 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
RMI FEMORAL VENOUS DRAINAGE CANNULA
| Applicant | Research Medical, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Feb 19, 1987 |
| Received | Sep 23, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863740
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.