ClearanceBrief
510(k) K852913 ยท

HGM ENDOCOAGULATOR MODEL 20

ApplicantHgm, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Sep 5, 1985
ReceivedJul 11, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K852913

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.