ClearanceBrief
510(k) K021299 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

CONMED HEATWAVE HAND-CONTROLLED ELETRODE

ApplicantConmedcorp, Utica NY, US
DecisionSubstantially Equivalent, Jun 26, 2002
ReceivedApr 24, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021299

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.