ClearanceBrief
510(k) K002002 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

SUREFIT DISPERSIVE ELECTRODE

ApplicantConmedcorp, Utica NY, US
DecisionSubstantially Equivalent, Aug 17, 2000
ReceivedJun 30, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002002

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.