ClearanceBrief
510(k) K151645 ยท MUE Full Field Digital, System, X-Ray, Mammographic

MAMMOMAT Fusion

ApplicantSiemens Medical Solutions USA, Inc., Mavern PA, US
DecisionSubstantially Equivalent, Sep 14, 2015
ReceivedJun 18, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K151645

DateFirm and productCodeLinked 510(k)
Dec 3, 2025Siemens Medical Solutions USA, Inc
MAMMOMAT Fusion;
Open, Classified
MUENone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.