ClearanceBrief
510(k) K103730 ยท KGI Densitometer, Bone

GE LUNAR VISCERAL FAT SOFTWARE

ApplicantGe Medical Systems Ultrasound and Primary Care Dia, Madison WI, US
DecisionSubstantially Equivalent, May 6, 2011
ReceivedDec 21, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K103730

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.