ClearanceBrief
510(k) K250370 ยท JAK System, X-Ray, Tomography, Computed

SCENARIA View Phase 5.0

ApplicantFujifilm Corporation, Minato-Ku, JP
DecisionSubstantially Equivalent, May 20, 2025
ReceivedFeb 10, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K250370

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.