510(k) K223469 · FGE Stents, Drains And Dilators For The Biliary Ducts
WallFlex Biliary RX Stent System
| Applicant | Boston Scientific Corporation, Marlboro MA, US |
| Decision | Unknown, Jun 15, 2023 |
| Received | Nov 17, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223469
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.