510(k) K181669 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
ConvertX Biliary Stent System
| Applicant | Brightwater Medical, Dunlap IL, US |
| Decision | Substantially Equivalent, Mar 14, 2019 |
| Received | Jun 25, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181669
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.