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FDA 510(k)

CorNeat EverPatch

K-Number: K223074 · 2023-06-02

ApplicantCorneat Vision , Ltd.
Decision Date2023-06-02
Product CodeQWU
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CorNeat EverPatch is a medical device manufactured by Corneat Vision , Ltd.. It received FDA 510(k) clearance on 2023-06-02 under approval number K223074. The device is classified under product code QWU. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CorNeat EverPatch?

CorNeat EverPatch is a medical device that received FDA 510(k) clearance on 2023-06-02. It is manufactured by Corneat Vision , Ltd.. The 510(k) number is K223074.

When was CorNeat EverPatch approved by the FDA?

CorNeat EverPatch received FDA 510(k) clearance on 2023-06-02, under approval number K223074.

What company makes CorNeat EverPatch?

CorNeat EverPatch is manufactured by Corneat Vision , Ltd..

What is the FDA product code for CorNeat EverPatch?

The FDA product code for CorNeat EverPatch is QWU.

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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