ClearanceBrief
510(k) K181609 ยท PGY Display, Diagnostic Radiology

RadiForce GX560, GX560-AR

ApplicantEizo Corporation, Hakusan, JP
DecisionSubstantially Equivalent, Aug 24, 2018
ReceivedJun 19, 2018
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K181609

DateFirm and productCodeLinked 510(k)
Jul 30, 2019Eizo Corporation
RadiForce GX560 monochrome LCD monitor, models 0FTD2347 and 0FTD2379 - Product Usage: is indicated for use in displaying radiological images (including full-field digital mammography and digital breas
Open, Classified
PGYNone listed

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