510(k) K962899 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
ULTRAFLEX DIAMOND
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, May 20, 1997 |
| Received | Jul 25, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962899
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.