510(k) K880887 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
NEOCATH
| Applicant | Taris Corp., Fernandina Beach FL, US |
| Decision | Substantially Equivalent, May 24, 1988 |
| Received | Mar 2, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880887
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.