ClearanceBrief
510(k) K880404 ยท KGI Densitometer, Bone

CSI/QCT

ApplicantColumbia Scientific, Inc., Columbia MD, US
DecisionSubstantially Equivalent, Nov 17, 1988
ReceivedJan 29, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880404

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.