510(k) K011817 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
BRIDGE FX
| Applicant | Medtronic Ave, Inc., Santa Rosa CA, US |
| Decision | Unknown, Aug 22, 2001 |
| Received | Jun 11, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K011817
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.