510(k) K053454 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
RX HERCULINK ELITE BILIARY STENT SYSTEM
| Applicant | Guidant Corporation, Santa Clara CA, US |
| Decision | Unknown, Mar 6, 2006 |
| Received | Dec 9, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053454
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.