ClearanceBrief
510(k) K220583 ยท IYE Accelerator, Linear, Medical

ClearCheck Model RADCC V2

ApplicantRadformation, Inc., New York NY, US
DecisionSubstantially Equivalent, Aug 23, 2022
ReceivedMar 1, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220583

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.