ClearanceBrief
510(k) K212291 ยท IZL System, X-Ray, Mobile

PHOENIX

ApplicantSedecal., Sa., Algete, ES
DecisionSubstantially Equivalent, Sep 14, 2021
ReceivedJul 22, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K212291

DateFirm and productCodeLinked 510(k)
Mar 2, 2023SEDECAL SA
Phoenix mKDR, digital mobile diagnostic x-ray system
Open, Classified
IZLNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.