ClearanceBrief
510(k) K121816 ยท GXY Electrode, Cutaneous

SENSUS ELECTRODE

ApplicantNeurometrix, Inc., Waltham MA, US
DecisionSubstantially Equivalent, Nov 26, 2012
ReceivedJun 20, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121816

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.