510(k) K130792 ยท FGE Stents, Drains And Dilators For The Biliary Ducts
LIFESTENT BILIARY STENT SYSTEM, LIFESTENT XL BILIARY STENT SYSTEM
| Applicant | C.R. Bard, Inc., Tempe AZ, US |
| Decision | Unknown, Aug 30, 2013 |
| Received | Mar 22, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130792
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.