隐形眼镜，正畸，过夜佩戴
PMA编号：P050031 · 2022-05-10
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决定日期2022-05-10
PMA 编号P050031
产品代码NUU
设备分类第3类
医疗专科O
法规编号21 CFR 8
咨询委员会OP
请注意，由于您没有提供具体的医疗设备监管文本，我无法进行翻译。请提供具体的文本内容，以便我能够按照您的要求进行翻译。
器械摘要
Lens, contact, orthokeratology, overnight is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 2022-05-10. The device is classified under product code NUU. It was reviewed by the OP advisory panel.
常见问题
What is the Lens, contact, orthokeratology, overnight?
Lens, contact, orthokeratology, overnight is a medical device that received FDA 510(k) clearance on 2022-05-10. The listed applicant is CooperVision, Inc..
When did Lens, contact, orthokeratology, overnight receive FDA 510(k) clearance?
The clearance date for Lens, contact, orthokeratology, overnight can be found in the official FDA records.
Lens、接触镜、角膜塑形镜、过夜使用的申请人是谁？
The FDA 510(k) record lists CooperVision, Inc. as the applicant. This does not by itself establish the device manufacturer.
什么是FDA隐形眼镜、接触镜、角膜塑形镜、过夜使用的产品代码？
FDA产品代码，对于隐形眼镜、接触镜、正畸学、过夜使用的，为NUU。
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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