ClearanceBrief
510(k) K113725 ยท KGI Densitometer, Bone

VIRTUOST

ApplicantO.N. Diagnostics, Berkeley CA, US
DecisionSubstantially Equivalent, Sep 13, 2012
ReceivedDec 19, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113725

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.