ClearanceBrief
510(k) K232367 · QIH Automated Radiological Image Processing Software

cmAngio® V1.0

ApplicantCuremetrix, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Oct 5, 2023
ReceivedAug 8, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232367

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.