FDA 510(k) Application Details - K220153

Device Classification Name	Stimulator, Electro-Acupuncture   More FDA Info for this Device
510(K) Number	K220153
Device Name	Stimulator, Electro-Acupuncture
Applicant	Bozhou Rongjian Medical Appliance Co.,Ltd. Jianghuai Supply Base, Zhongkai Group, Mengcheng County Bozhou 233500 CN Other 510(k) Applications for this Company
Contact	Wu Zhifang Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	BWK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/19/2022
Decision Date	03/18/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review