CorNeat EverPatch
K号: K223074 · 2023-06-02
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决定日期2023-06-02
产品代码QWU
咨询委员会OP
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决定实质等同
器械摘要
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.
常见问题
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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