FDA 510(k) Application Details - K982324

Device Classification Name	Stimulator, Nerve, Transcutaneous, For Pain Relief   More FDA Info for this Device
510(K) Number	K982324
Device Name	Stimulator, Nerve, Transcutaneous, For Pain Relief
Applicant	CHATTANOOGA GROUP, INC. 4717 ADAMS RD. P.O. BOX 4287 HIXSON, TN 37343 US Other 510(k) Applications for this Company
Contact	CHERYL G DYER 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	07/02/1998
Decision Date	02/01/1999
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