FDA 510(k) Application Details - K220503

Device Classification Name	Stimulator, Nerve, Transcutaneous, For Pain Relief   More FDA Info for this Device
510(K) Number	K220503
Device Name	Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant	WAT Medical Technology Inc. Room703-711, No.2 North Taoyuan Road Ningbo 315600 CN Other 510(k) Applications for this Company
Contact	Joe Xu Other 510(k) Applications for this Contact
Regulation Number	882.5890   More FDA Info for this Regulation Number
Classification Product Code	GZJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/22/2022
Decision Date	04/23/2022
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