510(k) K001258 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
BX TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Unknown, Jun 27, 2000 |
| Received | Apr 18, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K001258
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.