ClearanceBrief
510(k) K914404 ยท KGI Densitometer, Bone

ORTHO SOFTWARE USED W/LUNAR DPX/DPX-L/DPS-@ DESIT

ApplicantLunar, Madison WI, US
DecisionSubstantially Equivalent, Feb 27, 1992
ReceivedOct 3, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K914404

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.