ClearanceBrief
510(k) K261315 ยท KPS System, Tomography, Computed, Emission

Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7 (11364753);Symbia Pro.specta VA40 Family

ApplicantSiemens Medical Solutions USA, Inc., Knoxville TN, US
DecisionSubstantially Equivalent, May 21, 2026
ReceivedApr 21, 2026
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K261315

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.