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NEUROMETRIX ADVANCE

Page Type
Cleared 510(K)
510(k) Number
K070109
510(k) Type
Traditional
Applicant
Neurometrix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2008
Days to Decision
470 days
Submission Type
Summary

NEUROMETRIX ADVANCE

Page Type
Cleared 510(K)
510(k) Number
K070109
510(k) Type
Traditional
Applicant
Neurometrix, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2008
Days to Decision
470 days
Submission Type
Summary