ClearanceBrief
510(k) K261229 ยท JAK System, X-Ray, Tomography, Computed

SCENARIA View Phase 6.0

ApplicantFujifilm Corporation, Minato-Ku, JP
DecisionSubstantially Equivalent, Sep 18, 2026
ReceivedApr 15, 2026
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K261229

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.