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FDA 510(k)

Verily Numetric Retinal Camera

K-Number: K242508 · 2024-12-09

ApplicantVerily Life Sciences, LLC
Decision Date2024-12-09
Product CodeHKI
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Verily Numetric Retinal Camera is a medical device manufactured by Verily Life Sciences, LLC. It received FDA 510(k) clearance on 2024-12-09 under approval number K242508. The device is classified under product code HKI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Verily Numetric Retinal Camera?

Verily Numetric Retinal Camera is a medical device that received FDA 510(k) clearance on 2024-12-09. It is manufactured by Verily Life Sciences, LLC. The 510(k) number is K242508.

When was Verily Numetric Retinal Camera approved by the FDA?

Verily Numetric Retinal Camera received FDA 510(k) clearance on 2024-12-09, under approval number K242508.

What company makes Verily Numetric Retinal Camera?

Verily Numetric Retinal Camera is manufactured by Verily Life Sciences, LLC.

What is the FDA product code for Verily Numetric Retinal Camera?

The FDA product code for Verily Numetric Retinal Camera is HKI.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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