510(k) K041796 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
| Applicant | Cordis Corporation, Miami Lakes FL, US |
| Decision | Unknown, Aug 3, 2004 |
| Received | Jul 2, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041796
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.