FDA 510(k) Application Details - K233492

Device Classification Name	Stimulator, Muscle, Powered, For Muscle Conditioning   More FDA Info for this Device
510(K) Number	K233492
Device Name	Stimulator, Muscle, Powered, For Muscle Conditioning
Applicant	Xiamen Comfier Technology Co., Ltd 2/F,3/F,4/F,5/F, No.65 Sunban South Road, Jimei District Xiamen 361012 CN Other 510(k) Applications for this Company
Contact	Petoula N/A Other 510(k) Applications for this Contact
Regulation Number	890.5850   More FDA Info for this Regulation Number
Classification Product Code	NGX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/30/2023
Decision Date	12/20/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review