ClearanceBrief
510(k) K203345 ยท KPR System, X-Ray, Stationary

MULTIX Impact

ApplicantSiemens Medical Solutions USA, Inc., Malvern PA, US
DecisionSubstantially Equivalent, Jan 7, 2021
ReceivedNov 13, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203345

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.