FDA 510(k)

Smart Pain Reliever, Model LT5019

K号: K162479 · 2017-02-08

申请人Shenzhen Dongdixin Technology Co., Ltd.

决定日期2017-02-08

产品代码NUH

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决定实质等同

器械摘要

Smart Pain Reliever, Model LT5019 is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Dongdixin Technology Co., Ltd.. It received FDA 510(k) clearance on 2017-02-08 under 510(k) number K162479. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Smart Pain Reliever, Model LT5019?

Smart Pain Reliever, Model LT5019 is a medical device that received FDA 510(k) clearance on 2017-02-08. The listed applicant is Shenzhen Dongdixin Technology Co., Ltd.. The 510(k) number is K162479.

When did Smart Pain Reliever, Model LT5019 receive FDA 510(k) clearance?

Smart Pain Reliever, Model LT5019 received FDA 510(k) clearance on 2017-02-08, under 510(k) number K162479.

Who is the listed applicant for Smart Pain Reliever, Model LT5019?

The FDA 510(k) record lists Shenzhen Dongdixin Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Smart Pain Reliever, Model LT5019?

The FDA product code for Smart Pain Reliever, Model LT5019 is NUH.

列明Shenzhen Dongdixin Technology Co., Ltd.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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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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