FDA 510(k) Application Details - K130723

Device Classification Name	Stimulator, Muscle, Powered, For Muscle Conditioning   More FDA Info for this Device
510(K) Number	K130723
Device Name	Stimulator, Muscle, Powered, For Muscle Conditioning
Applicant	FAMIDOC TECHNOLOGY CO., LTD No.212 Yilong Road, Hexi Industrial Zone, Jinxia, Changan Town Dongguan 523853 CN Other 510(k) Applications for this Company
Contact	REANNY WANG 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	03/18/2013
Decision Date	02/07/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review