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FDA 510(k)

Avaira活力(fanfilcon A)软(亲水)隐形眼镜

K号: K160803 · 2016-07-13

决定日期2016-07-13
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

Avaira Vitality (fanfilcon A) Soft (Hydrofilic) Contact Lens is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 2016-07-13 under 510(k) number K160803. 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 Avaira Vitality (fanfilcon A) Soft (Hydrofilic) Contact Lens?

Avaira Vitality (fanfilcon A) Soft (Hydrofilic) Contact Lens is a medical device that received FDA 510(k) clearance on 2016-07-13. The listed applicant is CooperVision, Inc.. The 510(k) number is K160803.

When did Avaira Vitality (fanfilcon A) Soft (Hydrofilic) Contact Lens receive FDA 510(k) clearance?

Avaira Vitality (fanfilcon A) Soft (Hydrofilic) Contact Lens received FDA 510(k) clearance on 2016-07-13, under 510(k) number K160803.

Who is the listed applicant for Avaira Vitality (fanfilcon A) Soft (Hydrofilic) Contact Lens?

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 Avaira Vitality (fanfilcon A) Soft (Hydrofilic) Contact Lens?

The FDA product code for Avaira Vitality (fanfilcon A) Soft (Hydrofilic) Contact Lens is LPL.

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列明CooperVision, Inc.为申报人的其他记录

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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。

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