ClearanceBrief
510(k) K261380 ยท QKQ Digital Pathology Image Viewing And Management Software

Concentriq AP-Dx

ApplicantProscia, Inc., Philadelphia PA, US
DecisionSubstantially Equivalent, Aug 5, 2026
ReceivedApr 27, 2026
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K261380

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.