FDA 510(k)

针刺激器

K号: K202861 · 2021-08-27

申请人Wuxi Jiajian Medical Instrument Co., Ltd.

决定日期2021-08-27

产品代码BWK

决定实质等同

器械摘要

Needle Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Wuxi Jiajian Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2021-08-27 under 510(k) number K202861. The device is classified under product code BWK. FDA Decision: Substantially Equivalent.

常见问题

What is the Needle Stimulator?

Needle Stimulator is a medical device that received FDA 510(k) clearance on 2021-08-27. The listed applicant is Wuxi Jiajian Medical Instrument Co., Ltd.. The 510(k) number is K202861.

When did Needle Stimulator receive FDA 510(k) clearance?

Needle Stimulator received FDA 510(k) clearance on 2021-08-27, under 510(k) number K202861.

Who is the listed applicant for Needle Stimulator?

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

What is the FDA product code for Needle Stimulator?

The FDA product code for Needle Stimulator is BWK.

列明Wuxi Jiajian Medical Instrument 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。

K244030针刺激器（CMNS6-1 PLUS, CMNS6-3）K231425经皮神经电刺激器（TENS WMPS2-1）K222879经皮神经电刺激器（型号：TENS WMPS6-1）K202893经皮神经电刺激器 K192568嘉健自粘电极

官方来源

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