FDA 510(k) Application Details - K041604

Device Classification Name	Electrode, Depth   More FDA Info for this Device
510(K) Number	K041604
Device Name	Electrode, Depth
Applicant	AD-TECH MEDICAL INSTRUMENT CORP. 800 LEVANGER LANE STOUGHTON, WI 53589 US Other 510(k) Applications for this Company
Contact	Gary Syring Other 510(k) Applications for this Contact
Regulation Number	882.1330   More FDA Info for this Regulation Number
Classification Product Code	GZL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/14/2004
Decision Date	08/16/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review