ClearanceBrief
510(k) K923993 ยท FGE Stents, Drains And Dilators For The Biliary Ducts

WALLSTENT BILIARY ENDOPROTHESES

ApplicantSchneider U.S. Stent Div., Plymouth MN, US
DecisionSubstantially Equivalent, Sep 30, 1994
ReceivedAug 10, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923993

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.