FDA 510(k) Application Details - K051128

Device Classification Name	Stimulator, Nerve, Transcutaneous, For Pain Relief   More FDA Info for this Device
510(K) Number	K051128
Device Name	Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant	PAIN RELIEF TECHNOLOGIES 15440 N. 71ST STREET #215 SCOTTSDALE, AZ 85254 US Other 510(k) Applications for this Company
Contact	KENDALL GORHAM 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	05/03/2005
Decision Date	03/10/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review