ClearanceBrief
510(k) K083818 ยท GXY Electrode, Cutaneous

UNIVERSAL ELECTRODES

ApplicantNeurometrix, Inc., Waltham MA, US
DecisionSubstantially Equivalent, Jan 21, 2009
ReceivedDec 22, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K083818

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.