FDA 510(k) Application Details - K082377

Device Classification Name	Stimulator, Nerve, Transcutaneous, For Pain Relief   More FDA Info for this Device
510(K) Number	K082377
Device Name	Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant	TENSCARE LTD 9 BLENHEIM ROAD EPSOM KT19 9BE GB Other 510(k) Applications for this Company
Contact	ANTHONY JANKEL Other 510(k) Applications for this Contact
Regulation Number	882.5890   More FDA Info for this Regulation Number
Classification Product Code	GZJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/18/2008
Decision Date	02/09/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review