EyeBOX— 510(k) K201841

Substantially Equivalent

Oculogica, Inc.

FDA 510(k) clearance K201841 for EyeBOX, Substantially Equivalent on 2020-09-06. Applicant: Oculogica, Inc..

Clearance details

Applicant: Oculogica, Inc.
Product code: Code QEA
Advisory panel: Neurology
Date received: 2020-07-02
Decision date: 2020-09-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

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