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FDA 510(k)

AQUASPLASH(聚甲基丙烯酸甲酯)软性(亲水性)日戴隐形眼镜

K号: K210609 · 2021-04-27

申请人Vp Optics
决定日期2021-04-27
产品代码LPL
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。
决定实质等同

器械摘要

AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens is the device name listed in this FDA 510(k) record. The listed applicant is Vp Optics. It received FDA 510(k) clearance on 2021-04-27 under 510(k) number K210609. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens?

AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens is a medical device that received FDA 510(k) clearance on 2021-04-27. The listed applicant is Vp Optics. The 510(k) number is K210609.

When did AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens receive FDA 510(k) clearance?

AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens received FDA 510(k) clearance on 2021-04-27, under 510(k) number K210609.

Who is the listed applicant for AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens?

The FDA 510(k) record lists Vp Optics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens?

The FDA product code for AQUASPLASH (Polymacon) Soft (Hydrophilic) Daily Wear Contact Lens is LPL.

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。

相关器械(代码:LPL)

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

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