ClearanceBrief
510(k) K251792 · DXX System, Catheter Control, Steerable

Stereotaxis GenesisX RMN with Navigant ™ Workstation (NWS)

ApplicantStereotaxis, Inc., Saint Louis MO, US
DecisionSubstantially Equivalent, Nov 6, 2025
ReceivedJun 11, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K251792

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.