SENSUS— 510(k) K130919

Substantially Equivalent

Neurometrix, Inc.

FDA 510(k) clearance K130919 for SENSUS, Substantially Equivalent on 2013-07-02. Applicant: Neurometrix, Inc..

Clearance details

Applicant: Neurometrix, Inc.
Product code: Code GZJ
Advisory panel: Neurology
Date received: 2013-04-03
Decision date: 2013-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waltham, MA, US

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