FDA 510(k)

デジタルTENSユニット

K番号: K170145 · 2017-04-29

決定日2017-04-29

製品コードNUH

諮問委員会NE

決定Substantially Equivalent

医療機器の概要

Digital TENS Unit is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Eapply Technology Co., Ltd.. It received FDA 510(k) clearance on 2017-04-29 under 510(k) number K170145. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Digital TENS Unit?

Digital TENS Unit is a medical device that received FDA 510(k) clearance on 2017-04-29. The listed applicant is Shenzhen Eapply Technology Co., Ltd.. The 510(k) number is K170145.

When did Digital TENS Unit receive FDA 510(k) clearance?

Digital TENS Unit received FDA 510(k) clearance on 2017-04-29, under 510(k) number K170145.

Who is the listed applicant for Digital TENS Unit?

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

What is the FDA product code for Digital TENS Unit?

The FDA product code for Digital TENS Unit is NUH.

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医療機器の概要

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関連機器（コード：NUH）

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