FDA 510(k) Applications Submitted by Oculogica, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K191183 05/02/2019 EyeBOX Oculogica, Inc.
K201841 07/02/2020 EyeBOX Oculogica, Inc.
K212310 07/23/2021 EyeBOX (Model EBX-4) Oculogica, Inc.
DEN170091 12/22/2017 EyeBOX Oculogica, Inc.


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