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FDA 510(k)

电除汗剂,电除汗剂敏感型,电除汗剂 ELITE

K号: K170835 · 2018-06-15

决定日期2018-06-15
产品代码EGJ
咨询委员会PM 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

Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE is the device name listed in this FDA 510(k) record. The listed applicant is Hightech Development. It received FDA 510(k) clearance on 2018-06-15 under 510(k) number K170835. The device is classified under product code EGJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE?

Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE is a medical device that received FDA 510(k) clearance on 2018-06-15. The listed applicant is Hightech Development. The 510(k) number is K170835.

When did Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE receive FDA 510(k) clearance?

Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE received FDA 510(k) clearance on 2018-06-15, under 510(k) number K170835.

Who is the listed applicant for Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE?

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

What is the FDA product code for Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE?

The FDA product code for Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE is EGJ.

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相关器械(代码:EGJ)

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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