510(k) K014205 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
MODIFICATION TO BRIDGE SELF-EXPANDING BILIARY STENT DELIVERY SYSTEM (BRIDGE SE)
| Applicant | Medtronic Ave, Inc., Santa Rosa CA, US |
| Decision | Unknown, Jan 14, 2002 |
| Received | Dec 21, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K014205
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.