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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 K172834
Device Name Dual output digital therapy massager
Applicant
Shenzhen Osto Technology Co., Ltd.
#43 Longfeng Rd., Xinsheng Community
Longgang St. Longgang District
Shenzhen,  CN
Applicant Contact Li Yang
Correspondent
Guangzhou GLOMED Biological Technology Co., Ltd.
Suite 306, Kecheng Mansion, #121 Science Rd.
Guangzhou Science Park
Guangzhou,  CN 510006
Correspondent Contact Cecilia Ceng
Regulation Number882.5890
Classification Product Code
NUH  
Subsequent Product Code
NGX  
Date Received09/19/2017
Decision Date 09/06/2018
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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