510(k) K863558 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
URESIL CAROTID SHUNT
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Nov 24, 1986 |
| Received | Sep 12, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863558
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.