ClearanceBrief
510(k) K220402 ยท KGI Densitometer, Bone

VirtuOst

ApplicantO.N. Diagnostics, Berkeley CA, US
DecisionSubstantially Equivalent, May 19, 2023
ReceivedFeb 11, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220402

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.