510(k) K983075 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
GUIDANT MEGALINK BILIARY STENT, MODEL #'S 1002949-18, 1002949-28, 1002949-38
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Unknown, Mar 3, 1999 |
| Received | Sep 2, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983075
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.