ClearanceBrief
510(k) K070109 ยท JXE Device, Nerve Conduction Velocity Measurement

NEUROMETRIX ADVANCE

ApplicantNeurometrix, Inc., Waltham MA, US
DecisionSubstantially Equivalent, Apr 25, 2008
ReceivedJan 11, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070109

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.