EyeBOX— 510(k) DEN170091

Unknown

Oculogica, Inc.

FDA 510(k) clearance DEN170091 for EyeBOX, Unknown on 2018-12-28. Applicant: Oculogica, Inc.. Device class: 2.

Clearance details

Applicant: Oculogica, Inc.
Product code: Code QEA
Device class: Class 2
Regulation: 21 CFR 882.1455
Advisory panel: Neurology
Date received: 2017-12-22
Decision date: 2018-12-28
Decision: Unknown
Clearance type: Direct
Location: New York, NY, US

View on FDA.gov ↗

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More clearances from Oculogica, Inc.

K191183 — EyeBOX2019-07-31

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