FDA 510(k) Application Details - K110509

Device Classification Name	Interferential Current Therapy   More FDA Info for this Device
510(K) Number	K110509
Device Name	Interferential Current Therapy
Applicant	EVERYWAY MEDICAL INSTRUMENTS CO., LTD. 845 ARONSON LAKE COURT ROSWELL, GA 30075 US Other 510(k) Applications for this Company
Contact	JAY MANSOUR Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/22/2011
Decision Date	06/20/2011
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