FDA 510(k) Application Details - K081998

Device Classification Name	Stimulator, Muscle, Powered, For Muscle Conditioning   More FDA Info for this Device
510(K) Number	K081998
Device Name	Stimulator, Muscle, Powered, For Muscle Conditioning
Applicant	ELECTRONIC WAVEFORM LABORATORY, INC. 16168 BEACH BLVD., SUITE 232 HUNTINGTON BEACH, CA 92647 US Other 510(k) Applications for this Company
Contact	RYAN P HEANEY 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	07/14/2008
Decision Date	07/09/2009
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