ClearanceBrief
510(k) K240301 · QDQ Radiological Computer Assisted Detection/Diagnosis Software For Lesions Suspicious For Cancer

MammoScreen® (3)

ApplicantTherapixel, Nice, FR
DecisionSubstantially Equivalent, Aug 1, 2024
ReceivedFeb 1, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240301

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.