ClearanceBrief
510(k) K855142 ยท FGE Stents, Drains And Dilators For The Biliary Ducts

ANGIOMED PERCUTANEOUS TRANSHEPATIC CHOLANGIOGTAPHY

ApplicantAngiomed U.S., Inc., Anaheim CA, US
DecisionSubstantially Equivalent, Mar 11, 1986
ReceivedDec 26, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K855142

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.