ClearanceBrief
510(k) K250241 ยท OWB Interventional Fluoroscopic X-Ray System

Cios Select

ApplicantSiemens Medical Solutions USA, Inc., Malvern PA, US
DecisionSubstantially Equivalent, Nov 4, 2025
ReceivedJan 27, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K250241

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.