ClearanceBrief
510(k) K230684 ยท PGY Display, Diagnostic Radiology

RadiForce MX217

ApplicantEizo Corporation, Hakusan, JP
DecisionSubstantially Equivalent, May 12, 2023
ReceivedMar 13, 2023
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K230684

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.