ClearanceBrief
510(k) K230839 ยท PSY Whole Slide Imaging System

Concentriq Dx

ApplicantProscia, Inc., Philadelphia PA, US
DecisionSubstantially Equivalent, Feb 8, 2024
ReceivedMar 27, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230839

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.