ClearanceBrief
510(k) K851651 ยท

HGM ENDOCOAGULATOR MODEL 8

ApplicantHgm, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Jul 23, 1985
ReceivedApr 22, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851651

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.