SENSUS— 510(k) K121184

Substantially Equivalent

Neurometrix, Inc.

FDA 510(k) clearance K121184 for SENSUS, Substantially Equivalent on 2012-08-02. Applicant: Neurometrix, Inc.. Device class: 2.

Clearance details

Applicant: Neurometrix, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2012-04-18
Decision date: 2012-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

Download summary PDF View on FDA.gov ↗

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