ClearanceBrief
510(k) K212616 ยท POK Computer-Assisted Diagnostic Software For Lesions Suspicious For Cancer

Koios DS

ApplicantKoios Medical, Inc., New York NY, US
DecisionSubstantially Equivalent, Dec 16, 2021
ReceivedAug 18, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K212616

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.