ClearanceBrief
510(k) K103485 ยท MUE Full Field Digital, System, X-Ray, Mammographic

SENOGRAPH DS, SENOGRAPH ESSENSTIAL

ApplicantGeneral Electric Company, Waukesha WI, US
DecisionSubstantially Equivalent, Oct 6, 2011
ReceivedNov 26, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K103485

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.