ClearanceBrief
510(k) K243391 ยท QKQ Digital Pathology Image Viewing And Management Software

AISight Dx

ApplicantPathAI, Inc., Boston MA, US
DecisionSubstantially Equivalent, Jun 26, 2025
ReceivedOct 31, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K243391

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.