ClearanceBrief
510(k) K254122 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

FLOW FLEXTEND Wand (72290039)

ApplicantArthroCare Corporation, Austin TX, US
DecisionSubstantially Equivalent, Mar 30, 2026
ReceivedDec 19, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K254122

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.