ClearanceBrief
510(k) K230370 ยท JAK System, X-Ray, Tomography, Computed

SpotLight/SpotLight Duo (with DLIR option)

ApplicantArineta , Ltd., Caesarea, IL
DecisionSubstantially Equivalent, Oct 13, 2023
ReceivedFeb 10, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230370

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.