510(k) K003929 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
NIROYAL BILIARY PREMOUNTED STENT SYSTEM
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Unknown, Mar 22, 2001 |
| Received | Dec 20, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003929
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.