510(k) K032436 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
DURAMAX .018 BILIARY STENT SYSTEM
| Applicant | Avantec Vascular Corp., Sunnyvale CA, US |
| Decision | Unknown, Feb 4, 2004 |
| Received | Aug 7, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032436
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.