ClearanceBrief
510(k) K182591 ยท PGY Display, Diagnostic Radiology

RadiForce RX360, RX360-AR

ApplicantEizo Corporation, Hakusan, JP
DecisionSubstantially Equivalent, Oct 18, 2018
ReceivedSep 20, 2018
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K182591

DateFirm and productCodeLinked 510(k)
Jul 30, 2019Eizo Corporation
RadiForce RX360, model 0FTD2346 - Product Usage: is a color LCD monitor indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The di
Open, Classified
PGYNone listed

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