510(k) K980823 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
CORDIS NITINOL STENT AND DELIVERY SYSTEM
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Unknown, Dec 18, 1998 |
| Received | Mar 3, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980823
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.