510(k) K955818 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
FOAMSEAL RETROGRADE CARDIOPLEGIA CATHETER
| Applicant | Quest Medical, Inc., Allen TX, US |
| Decision | Substantially Equivalent, Mar 26, 1996 |
| Received | Dec 26, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955818
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.