TENS Device-EmeTerm, CinvStop

Stimulator, Nerve, Transcutaneous, For Pain Relief

WAT Medical Technology (Ningbo) Co., Ltd

The following data is part of a premarket notification filed by Wat Medical Technology (ningbo) Co., Ltd with the FDA for Tens Device-emeterm, Cinvstop.

Pre-market Notification Details

Device IDK172478
510k NumberK172478
Device Name:TENS Device-EmeTerm, CinvStop
ClassificationStimulator, Nerve, Transcutaneous, For Pain Relief
Applicant WAT Medical Technology (Ningbo) Co., Ltd Room703-711, No.2 North Taoyuan Road Ningbo,  CN 315600
ContactRodney Zhang
CorrespondentRodney Zhang
WAT Medical Technology (Ningbo) Co., Ltd Room703-711, No.2 North Taoyuan Road Ningbo,  CN 315600
Product CodeGZJ  
CFR Regulation Number882.5890 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2017-08-16
Decision Date2018-04-19
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
06971760280015 K172478 000
16971760280074 K172478 000
16971760280081 K172478 000
16971760280098 K172478 000
16971760280104 K172478 000
16971760281125 K172478 000
06971760280251 K172478 000
16971760281071 K172478 000
16971760281309 K172478 000
16971760281019 K172478 000
16971760281033 K172478 000
16971760281088 K172478 000
16971760280067 K172478 000

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