510(k) K030638 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
DURAMAX .035 BILIARY STENT SYSTEM, MODELS DML0718-80, DML0718-135, DML0818-80, DML0818-135, DML0918-80, DML0918-135, DML
| Applicant | Avantec Vascular Corp., Sunnyvale CA, US |
| Decision | Unknown, Jul 9, 2003 |
| Received | Feb 28, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030638
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.