FDA 510(k) Application Details - K990230

Device Classification Name	Stimulator, Nerve, Transcutaneous, For Pain Relief   More FDA Info for this Device
510(K) Number	K990230
Device Name	Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant	BIOMEDICAL LIFE SYSTEMS, INC. 2448 CADES WAY VISTA, CA 92083 US Other 510(k) Applications for this Company
Contact	RICHARD SAXON 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	01/25/1999
Decision Date	08/19/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review