FDA 510(k)

Nix Ultra虱子治疗套装

K号: K163401 · 2017-03-21

决定日期2017-03-21

产品代码LJL

咨询委员会医疗设备监管文本翻译如下： HO 请注意，由于您没有提供具体的医疗设备监管文本内容，以上仅为示例。请提供具体的文本内容以便进行准确的翻译。

决定实质等同

器械摘要

Nix Ultra Lice Treatment Kit is the device name listed in this FDA 510(k) record. The listed applicant is Medtech Products, Inc.. It received FDA 510(k) clearance on 2017-03-21 under 510(k) number K163401. The device is classified under product code LJL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Nix Ultra Lice Treatment Kit?

Nix Ultra Lice Treatment Kit is a medical device that received FDA 510(k) clearance on 2017-03-21. The listed applicant is Medtech Products, Inc.. The 510(k) number is K163401.

When did Nix Ultra Lice Treatment Kit receive FDA 510(k) clearance?

Nix Ultra Lice Treatment Kit received FDA 510(k) clearance on 2017-03-21, under 510(k) number K163401.

Who is the listed applicant for Nix Ultra Lice Treatment Kit?

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

What is the FDA product code for Nix Ultra Lice Treatment Kit?

The FDA product code for Nix Ultra Lice Treatment Kit is LJL.

列明Medtech Products, Inc.为申报人的其他记录

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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