ClearanceBrief
510(k) K021986 ยท GXY Electrode, Cutaneous

BRAINET

ApplicantNicolet Biomedical, Inc., Stoughton WI, US
DecisionSubstantially Equivalent, Aug 23, 2002
ReceivedJun 18, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021986

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.