ClearanceBrief
510(k) K233925 ยท QIH Automated Radiological Image Processing Software

Relu Creator

ApplicantRelu BV, Leuven, BE
DecisionSubstantially Equivalent, Jun 13, 2024
ReceivedDec 13, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233925

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.