510(k) K250784

Device
Transcutaneous Electrical Nerve Stimulator ( K6133/ K6134/ K6135/ K6136/ K6137/ K6138/ K6139/ K6140/ K6141/ K6142/ K6143/ K6144/ K6122)
Applicant
Shenzhen Yicai Health Technology Co., Ltd.
510(k) number
K250784
Product code
NUH
Decision
Substantially Equivalent (SESE)
Decision date
2025-08-21
Date received
2025-03-14
Regulation
882.5890
Classification name
Stimulator, Nerve, Transcutaneous, Over-The-Counter
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Jie Xie
Address
11th Floor, Zhenqian Bldg., Yousong Community Longhua St., Longhua District Shenzhen CN 518110 518110

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

Other 510(k) Records For Product Code NUH

510(k)DeviceApplicantDecision date
K253896TENS/EMS device (GUSE01)Globalcare Medical Technology Co., Ltd.2026-03-04
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K243131Triathlon ProSigma Biomedical2025-11-07
K251429OTC 4-Channel Rechargeable TENS UnitChangsha Anxiang Medical Technology Co., Ltd.2025-08-28
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K243856TENS AND EMS (TENS and Muscle Stimulator) ( Model AS8012C,AS8016,AS8019,AS9020E,AS9026)Shenzhen Astec Technology Co., Ltd.2025-05-29
K250360TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026)Shenzhen Jiantuo Electronics Co., Ltd.2025-05-11
K250053TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B)Shenzhen Jiantuo Electronics Co., Ltd.2025-05-09
K243613Patch-TEA (Model TRI-21)Transtimulation Research, Inc.2025-04-09
K250033Smart Pulse Relief (PZ-2622, PZ-2622T, PZ-2622E)Guangzhou Pinzhi Medical Technology Co., Ltd.2025-04-07
K242460Progenix Select StimProgenix, LLC2025-04-02