510(k) K242508

Device
Verily Numetric Retinal Camera
Applicant
Verily Life Sciences, LLC
510(k) number
K242508
Product code
HKI
Decision
Substantially Equivalent (SESE)
Decision date
2024-12-09
Date received
2024-08-22
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
Yes

Applicant Contact#

Contact
Shah Pooja
Address
269 E. Grand Ave. South San Francisco CA US 94080 94080

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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