FDA 510(k) Application Details - K042912

Device Classification Name	Stimulator, Nerve, Transcutaneous, For Pain Relief   More FDA Info for this Device
510(K) Number	K042912
Device Name	Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant	NEURO RESOURCE GROUP, INC. 2220 CHEMSEARCH BLVD. SUITE 108 IRVING, TX 75062 US Other 510(k) Applications for this Company
Contact	KRISTA OAKES 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	10/21/2004
Decision Date	05/17/2005
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