ClearanceBrief
510(k) K915535 ยท KGI Densitometer, Bone

FOREARM SOFTWARE FOR LUNAR DPX SERIES BONE DESITOM

ApplicantLunar, Madison WI, US
DecisionSubstantially Equivalent, Feb 27, 1992
ReceivedDec 9, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915535

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.