FDA 510(k) Application Details - K962951

Device Classification Name	Stimulator, Nerve, Transcutaneous, For Pain Relief   More FDA Info for this Device
510(K) Number	K962951
Device Name	Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant	TECHNALITHICS LABORATORIES, INC. 7003 WOODWAY DR., SUITE 315 WACO, TX 76712 US Other 510(k) Applications for this Company
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	07/26/1996
Decision Date	08/06/1997
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