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FDA 510(k)

CorNeat EverPatch

N.º K: K223074 · 2023-06-02

SolicitanteCorneat Vision , Ltd.
Fecha de decisión2023-06-02
Código de productoQWU
Comité asesorOP
DecisiónSubstantially Equivalent

Resumen del dispositivo

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

Preguntas frecuentes

What is the CorNeat EverPatch?

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

When did CorNeat EverPatch receive FDA 510(k) clearance?

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

Who is the listed applicant for CorNeat EverPatch?

The FDA 510(k) record lists Corneat Vision , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CorNeat EverPatch?

The FDA product code for CorNeat EverPatch is QWU.

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Fuente oficial

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