ClearanceBrief
510(k) K861233 ยท KGI Densitometer, Bone

DUAL PHOTON BONE DENSITOMETER

ApplicantMedical and Scientific Enterprises, Inc., Concord MA, US
DecisionSubstantially Equivalent, Mar 3, 1987
ReceivedApr 1, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861233

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.