ClearanceBrief
510(k) K163252 ยท MUE Full Field Digital, System, X-Ray, Mammographic

Mammomat Fusion with Stereotactic Biopsy

ApplicantSiemens Medical Solutions USA, Inc., Malvern PA, US
DecisionSubstantially Equivalent, Jan 10, 2017
ReceivedNov 18, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K163252

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.