510(k) K053459 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
OMNILINK .035 BILIARY STENT SYSTEM
| Applicant | Guidant Corporation, Temecula CA, US |
| Decision | Unknown, Apr 12, 2006 |
| Received | Dec 13, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053459
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.