ClearanceBrief
510(k) K200726 ยท IZL System, X-Ray, Mobile

AcuityPDR

ApplicantRadmedix, LLC, Dayton OH, US
DecisionSubstantially Equivalent, Apr 13, 2020
ReceivedMar 20, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K200726

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.