510(k) K992319 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
RX MEGALINK SDS BILIARY STENT SYSTEM, OTW MEGALINK SDS BILIARY STENT SYSTEM
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Unknown, Oct 8, 1999 |
| Received | Jul 12, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992319
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.