Electro Auricular Device— 510(k) K140530

Name: FDA 510(k) clearance K140530
Creator: U.S. Food and Drug Administration
Published: 2014-10-02

Substantially Equivalent

Navigant Consulting, Inc.

FDA 510(k) clearance K140530 for Electro Auricular Device, Substantially Equivalent on 2014-10-02. Applicant: Navigant Consulting, Inc.. Device class: Unclassified.

Clearance details

Applicant: Navigant Consulting, Inc.
Product code: Code BWK
Device class: Unclassified
Advisory panel: Unknown
Date received: 2014-03-04
Decision date: 2014-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

Download summary PDF View on FDA.gov ↗

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