ClearanceBrief
510(k) K220919 ยท KPR System, X-Ray, Stationary

MULTIX Impact E

ApplicantSiemens Medical Solutions USA, Inc., Malvern PA, US
DecisionSubstantially Equivalent, May 17, 2022
ReceivedMar 30, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220919

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.