Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
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.
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact