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FDA 510(k)

Hidrocor, Hidrocharme, and Natural Colors

K号: K160472 · 2016-08-10

申请人Solotica
决定日期2016-08-10
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

Hidrocor, Hidrocharme, and Natural Colors is the device name listed in this FDA 510(k) record. The listed applicant is Solotica. It received FDA 510(k) clearance on 2016-08-10 under 510(k) number K160472. 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 Hidrocor, Hidrocharme, and Natural Colors?

Hidrocor, Hidrocharme, and Natural Colors is a medical device that received FDA 510(k) clearance on 2016-08-10. The listed applicant is Solotica. The 510(k) number is K160472.

When did Hidrocor, Hidrocharme, and Natural Colors receive FDA 510(k) clearance?

Hidrocor, Hidrocharme, and Natural Colors received FDA 510(k) clearance on 2016-08-10, under 510(k) number K160472.

Who is the listed applicant for Hidrocor, Hidrocharme, and Natural Colors?

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

What is the FDA product code for Hidrocor, Hidrocharme, and Natural Colors?

The FDA product code for Hidrocor, Hidrocharme, and Natural Colors is LPL.

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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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