FDA 510(k)

经皮神经电刺激（TENS）设备-EmeTerm，CinvStop

K号: K172478 · 2018-04-19

申请人Wat Medical Technology (Ningbo) Co., Ltd.

决定日期2018-04-19

产品代码GZJ

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决定实质等同

器械摘要

TENS device-EmeTerm, CinvStop is the device name listed in this FDA 510(k) record. The listed applicant is Wat Medical Technology (Ningbo) Co., Ltd.. It received FDA 510(k) clearance on 2018-04-19 under 510(k) number K172478. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the TENS device-EmeTerm, CinvStop?

TENS device-EmeTerm, CinvStop is a medical device that received FDA 510(k) clearance on 2018-04-19. The listed applicant is Wat Medical Technology (Ningbo) Co., Ltd.. The 510(k) number is K172478.

When did TENS device-EmeTerm, CinvStop receive FDA 510(k) clearance?

TENS device-EmeTerm, CinvStop received FDA 510(k) clearance on 2018-04-19, under 510(k) number K172478.

Who is the listed applicant for TENS device-EmeTerm, CinvStop?

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

What is the FDA product code for TENS device-EmeTerm, CinvStop?

The FDA product code for TENS device-EmeTerm, CinvStop is GZJ.

列明Wat Medical Technology (Ningbo) 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。

K172450经皮神经电刺激（TENS）设备-HeadaTerm，eEspress

官方来源

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