510(k) K880103 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPUL.
| Applicant | Research Medical, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Mar 22, 1988 |
| Received | Jan 12, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880103
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.