ClearanceBrief
510(k) K844835 ยท KGI Densitometer, Bone

ND2100 SPINE SCANNER

ApplicantNuclear Data, Inc., Schaumburg IL, US
DecisionSubstantially Equivalent, Apr 18, 1985
ReceivedDec 12, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K844835

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.