510(k) K113582 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
ARCHSTENT BILIARY SYSTEM
| Applicant | Ostial Corporation, Mountain View CA, US |
| Decision | Unknown, Jun 29, 2012 |
| Received | Dec 5, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113582
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.