ClearanceBrief
510(k) K885180 ยท FGE Stents, Drains And Dilators For The Biliary Ducts

EXPANDABLE BILIARY STENT ENDOPROSTHESIS

ApplicantSchneider Intl., Ltd., Minneapolis MN, US
DecisionSubstantially Equivalent, Feb 16, 1989
ReceivedDec 14, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K885180

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.