ClearanceBrief
510(k) K241200 ยท JAK System, X-Ray, Tomography, Computed

SpotLight/SpotLight Duo with Low Dose Lung Cancer Screening Option

ApplicantArineta , Ltd., Caesarea, IL
DecisionSubstantially Equivalent, Jan 13, 2025
ReceivedApr 30, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K241200

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.