ClearanceBrief
510(k) K950611 ยท KGI Densitometer, Bone

EXPERT MORPHOMERTY SOFTWARD

ApplicantLunar Corp., Madison WI, US
DecisionSubstantially Equivalent, May 24, 1995
ReceivedFeb 10, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950611

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.