ClearanceBrief
510(k) K203504 ยท OWB Interventional Fluoroscopic X-Ray System

Cios Flow

ApplicantSiemens Medical Solutions USA, Inc., Malvern PA, US
DecisionSubstantially Equivalent, Dec 22, 2020
ReceivedNov 30, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K203504

DateFirm and productCodeLinked 510(k)
Oct 27, 2023Siemens Medical Solutions USA, Inc
***Updated 12/4/23*** (1) Cios Flow (VA30) mobile fluoroscopic C-arm X-ray System. Designed for the surgical environment and provides comprehensive image acquisition modes. Material Number: 11108110
Open, Classified
OWBNone listed

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