FDA 510(k) Application Details - K220002

Device Classification Name	Electrode, Cutaneous   More FDA Info for this Device
510(K) Number	K220002
Device Name	Electrode, Cutaneous
Applicant	Zhejiang Qiangnao Technology Co.,Ltd Room 201-5, Building 1, No.1818-2, Wenyi West Road Yuhang Street, Yuhang District Hangzhou 310000 CN Other 510(k) Applications for this Company
Contact	Boyuan Meng Other 510(k) Applications for this Contact
Regulation Number	882.1320   More FDA Info for this Regulation Number
Classification Product Code	GXY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/04/2022
Decision Date	09/09/2022
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