ClearanceBrief
510(k) K223409 ยท OWB Interventional Fluoroscopic X-Ray System

Cios Select (VA21) Image Intensifier

ApplicantSiemens Medical Solutions USA, Inc., Malvern PA, US
DecisionSubstantially Equivalent, Dec 6, 2022
ReceivedNov 9, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K223409

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.