510(k) K881352 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
RIGHT ATRIAL CATHETER INSERTION TRAY
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Jun 9, 1988 |
| Received | Mar 30, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881352
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.