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FDA 510(k)

Everyway OTC经皮神经电刺激(TENS)/电肌肉刺激(EMS)组合

K号: K192589 · 2019-12-19

决定日期2019-12-19
产品代码NUH
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决定实质等同

器械摘要

Everyway OTC TENS/EMS Combination is the device name listed in this FDA 510(k) record. The listed applicant is Everyway Medical Instruments Co.,Ltd. It received FDA 510(k) clearance on 2019-12-19 under 510(k) number K192589. 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 Everyway OTC TENS/EMS Combination?

Everyway OTC TENS/EMS Combination is a medical device that received FDA 510(k) clearance on 2019-12-19. The listed applicant is Everyway Medical Instruments Co.,Ltd. The 510(k) number is K192589.

When did Everyway OTC TENS/EMS Combination receive FDA 510(k) clearance?

Everyway OTC TENS/EMS Combination received FDA 510(k) clearance on 2019-12-19, under 510(k) number K192589.

Who is the listed applicant for Everyway OTC TENS/EMS Combination?

The FDA 510(k) record lists Everyway Medical Instruments Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Everyway OTC TENS/EMS Combination?

The FDA product code for Everyway OTC TENS/EMS Combination is NUH.

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列明Everyway Medical Instruments Co.,Ltd为申报人的其他记录

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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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