ClearanceBrief
510(k) K250310 · DRF Catheter, Electrode Recording, Or Probe, Electrode Recording

VIKING™ Fixed Curve Diagnostic Catheter

ApplicantBoston Scientific Corporation, St Paul MN, US
DecisionSubstantially Equivalent, Jun 27, 2025
ReceivedFeb 3, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K250310

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.