510(k) K230627

Device
Zilia Ocular FC (ZIL-10002)
Applicant
Zilia, Inc.
510(k) number
K230627
Product code
HKI
Decision
Substantially Equivalent (SESE)
Decision date
2023-11-20
Date received
2023-03-06
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
No

Applicant Contact#

Contact
Sauvageau Patrick
Address
125 Charest Blvd. E. Suite 400 Quebec City CA G1K3G5 G1K3G5

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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