510(k) K012993 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
MODIFICATION TO PRECISE NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Unknown, Oct 5, 2001 |
| Received | Sep 6, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K012993
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.