ADHERENT VISUAL STIMULATOR GOGGLES— 510(k) K113785

Name: FDA 510(k) clearance K113785
Creator: U.S. Food and Drug Administration
Published: 2012-06-06

Substantially Equivalent

Anschel Technology, Inc.

FDA 510(k) clearance K113785 for ADHERENT VISUAL STIMULATOR GOGGLES, Substantially Equivalent on 2012-06-06. Applicant: Anschel Technology, Inc.. Device class: 2.

Clearance details

Applicant: Anschel Technology, Inc.
Product code: Code GWE
Device class: Class 2
Regulation: 21 CFR 882.1890
Advisory panel: Neurology
Date received: 2011-12-23
Decision date: 2012-06-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.