ClearanceBrief
510(k) K934040 ยท KGI Densitometer, Bone

THE OSTEOREPORT

ApplicantWoodson and Associates, LLC, Decatur GA, US
DecisionSubstantially Equivalent, Sep 26, 1994
ReceivedAug 18, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934040

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.