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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Nerve, Transcutaneous, Over-The-Counter
510(k) Number K190009
Device Name Sunmas TENS & PMS (Model SM9187, SM9180L, SM9180S)
Applicant
Hong Qiangxing (Shenzhen) Electronics Limited
4f, Jingcheng Bldg., Xicheng Industrial Zone,
Xixiang Rd., Bao'An District
Shenzhen,  CN 518126
Applicant Contact Xu Jianhua
Correspondent
Shanghai CV Technology Co., Ltd.
Rm. 903, #19 Dongbao Rd., Songjiang Area,
Shanghai,  CN 201613
Correspondent Contact Doris Dong
Regulation Number882.5890
Classification Product Code
NUH  
Subsequent Product Code
NGX  
Date Received01/03/2019
Decision Date 12/02/2019
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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