FDA 510(k) Application Details - K163611

Device Classification Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter   More FDA Info for this Device
510(K) Number	K163611
Device Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter
Applicant	Guangzhou Xinbo Electronic Co., Ltd. 2nd Building, Juntuo Industry Park, Xingye Dadao Nancun Town, Panyu District Guangzhou 511400 CN Other 510(k) Applications for this Company
Contact	Sammy Li Other 510(k) Applications for this Contact
Regulation Number	882.5890   More FDA Info for this Regulation Number
Classification Product Code	NUH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/22/2016
Decision Date	09/19/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review