ClearanceBrief
510(k) K033550 ยท KGI Densitometer, Bone

DXL CALSCAN

ApplicantDemetech AB, Solna, SE
DecisionSubstantially Equivalent, May 5, 2004
ReceivedNov 12, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033550

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.