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FDA 510(k)

椰子混合型

K号: K242162 · 2024-09-19

决定日期2024-09-19
产品代码NUC
咨询委员会OB 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

Coconut Hybrid is the device name listed in this FDA 510(k) record. The listed applicant is Good Clean Love, Inc.. It received FDA 510(k) clearance on 2024-09-19 under 510(k) number K242162. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Coconut Hybrid?

Coconut Hybrid is a medical device that received FDA 510(k) clearance on 2024-09-19. The listed applicant is Good Clean Love, Inc.. The 510(k) number is K242162.

When did Coconut Hybrid receive FDA 510(k) clearance?

Coconut Hybrid received FDA 510(k) clearance on 2024-09-19, under 510(k) number K242162.

Who is the listed applicant for Coconut Hybrid?

The FDA 510(k) record lists Good Clean Love, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Coconut Hybrid?

The FDA product code for Coconut Hybrid is NUC.

相关临床试验

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列明Good Clean Love, Inc.为申报人的其他记录

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相关器械(代码:NUC)

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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