510(k) K991032 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
GUIDANT MEGALINK BILIARY STENT, MODEL FG1002949-58
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Unknown, Apr 30, 1999 |
| Received | Mar 29, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K991032
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.