每日佩戴软性隐形眼镜以减缓近视进展
PMA编号：P180035 · 2026-02-17
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决定日期2026-02-17
PMA 编号P180035
产品代码QIT
设备分类第3类
医疗专科U
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
Daily wear soft contact lens to reduce the progression of myopia is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 2026-02-17. The device is classified under product code QIT. It was reviewed by the OP advisory panel.
常见问题
What is the Daily wear soft contact lens to reduce the progression of myopia?
Daily wear soft contact lens to reduce the progression of myopia is a medical device that received FDA 510(k) clearance on 2026-02-17. The listed applicant is CooperVision, Inc..
When did Daily wear soft contact lens to reduce the progression of myopia receive FDA 510(k) clearance?
The clearance date for Daily wear soft contact lens to reduce the progression of myopia can be found in the official FDA records.
Who is the listed applicant for Daily wear soft contact lens to reduce the progression of myopia?
The FDA 510(k) record lists CooperVision, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Daily wear soft contact lens to reduce the progression of myopia?
The FDA product code for Daily wear soft contact lens to reduce the progression of myopia is QIT.
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官方来源
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