ClearanceBrief
510(k) K792444 ยท KGI Densitometer, Bone

NORLAND MODEL 278 BONE DENSITOMETER

ApplicantNorland Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 27, 1979
ReceivedNov 29, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792444

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.