510(k) K955728 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
CORDIS BILIARY STENT
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, May 8, 1996 |
| Received | Dec 18, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955728
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.