NEUROMETRIX ADVANCE— 510(k) K070109

Substantially Equivalent

Neurometrix, Inc.

FDA 510(k) clearance K070109 for NEUROMETRIX ADVANCE, Substantially Equivalent on 2008-04-25. Applicant: Neurometrix, Inc.. Device class: 2.

Clearance details

Applicant: Neurometrix, Inc.
Product code: Code JXE
Device class: Class 2
Regulation: 21 CFR 882.1550
Advisory panel: Neurology
Date received: 2007-01-11
Decision date: 2008-04-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

Download summary PDF View on FDA.gov ↗

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