FDA 510(k) Application Details - K993229

Device Classification Name	Stimulator, Nerve, Transcutaneous, For Pain Relief   More FDA Info for this Device
510(K) Number	K993229
Device Name	Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant	JOHARI ELECTRO-TECH CO. VANDANA, 28 NEHRU PARK, JODHPUR-342003 342003 IN Other 510(k) Applications for this Company
Contact	NISHA JOHARI 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	09/27/1999
Decision Date	02/02/2001
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