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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name brain injury adjunctive interpretive oculomotor assessment aid
510(k) Number K201841
Device Name EyeBOX
Oculogica, Inc.
33 Irving Place
New York,  NY  10003
Applicant Contact Rosina Samadani
Hogan Lovells US LLP
1735 Market Street
Suite 2300
Philadelphia,  PA  19103
Correspondent Contact Janice Hogan
Regulation Number882.1455
Classification Product Code
Date Received07/02/2020
Decision Date 09/06/2020
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No