510(k) K872788 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
MODIFIED CAROTID SHUNT W/SPRING REINFORCED LUMEN
| Applicant | Uresil Corp., Skokie IL, US |
| Decision | Substantially Equivalent, Sep 25, 1987 |
| Received | Jul 14, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872788
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.