ClearanceBrief
510(k) K220105 ยท QDQ Radiological Computer Assisted Detection/Diagnosis Software For Lesions Suspicious For Cancer

Saige-Dx

ApplicantDeepHealth, Inc., Cambridge MA, US
DecisionSubstantially Equivalent, May 12, 2022
ReceivedJan 12, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220105

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.