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FDA 510(k)

经皮神经电刺激与经皮肌肉刺激(型号:SM9089, SM9587, SM9592, SM9555)

K号: K220152 · 2022-04-19

决定日期2022-04-19
产品代码NUH
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决定实质等同

器械摘要

TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555) is the device name listed in this FDA 510(k) record. The listed applicant is Hong Qiangxing (Shenzhen) Electronics Limited. It received FDA 510(k) clearance on 2022-04-19 under 510(k) number K220152. 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 TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555)?

TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555) is a medical device that received FDA 510(k) clearance on 2022-04-19. The listed applicant is Hong Qiangxing (Shenzhen) Electronics Limited. The 510(k) number is K220152.

When did TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555) receive FDA 510(k) clearance?

TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555) received FDA 510(k) clearance on 2022-04-19, under 510(k) number K220152.

Who is the listed applicant for TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555)?

The FDA 510(k) record lists Hong Qiangxing (Shenzhen) Electronics Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555)?

The FDA product code for TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555) is NUH.

相关临床试验

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列明Hong Qiangxing (Shenzhen) Electronics Limited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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相关器械(代码:NUH)

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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