510(k) K014184 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
MODIFICATION TO DYNALINK .035 BILIARY SELF-EXPANDING STENT SYSTEM
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Unknown, Jan 18, 2002 |
| Received | Dec 20, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K014184
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.