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FDA 510(k)

VERVE

K-Number: K232930 · 2024-06-13

ApplicantOculomotor Technologies
Decision Date2024-06-13
Product CodeSBN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VERVE is a medical device manufactured by Oculomotor Technologies. It received FDA 510(k) clearance on 2024-06-13 under approval number K232930. The device is classified under product code SBN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERVE?

VERVE is a medical device that received FDA 510(k) clearance on 2024-06-13. It is manufactured by Oculomotor Technologies. The 510(k) number is K232930.

When was VERVE approved by the FDA?

VERVE received FDA 510(k) clearance on 2024-06-13, under approval number K232930.

What company makes VERVE?

VERVE is manufactured by Oculomotor Technologies.

What is the FDA product code for VERVE?

The FDA product code for VERVE is SBN.

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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