ClearanceBrief
510(k) K021527 ยท KGI Densitometer, Bone

SECTRA OSTEOPOROSIS PACKAGE

ApplicantSectra-Imtec AB, Denton TX, US
DecisionSubstantially Equivalent, Jun 7, 2002
ReceivedMay 10, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K021527

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.