ClearanceBrief
510(k) K810159 ยท KGI Densitometer, Bone

BONE MINERAL ANALYZER CONTROLLER

ApplicantLunar Radiation Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 12, 1981
ReceivedJan 21, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810159

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.