510(k) K250770

Device
Optina-4C (MHRC-C1N)
Applicant
Optina Diagnostics, Inc.
510(k) number
K250770
Product code
HKI
Decision
Substantially Equivalent (SESE)
Decision date
2025-09-04
Date received
2025-03-13
Regulation
886.1120
Classification name
Camera, Ophthalmic, Ac-Powered
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Sarah Lemaire
Address
8200 Blvd. Decarie Montreal CA H4P 2P5 H4P 2P5

FDA Registration Numbers

Source Documents

510(k) summary PDF

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