FDA 510(k) Application Details - K040639

Device Classification Name	Electrode, Needle   More FDA Info for this Device
510(K) Number	K040639
Device Name	Electrode, Needle
Applicant	ISURGICAL 26625 COUNTRYSIDE LAKE DRIVE MUNDELEIN, IL 60060 US Other 510(k) Applications for this Company
Contact	KEN LEISER Other 510(k) Applications for this Contact
Regulation Number	882.1350   More FDA Info for this Regulation Number
Classification Product Code	GXZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/10/2004
Decision Date	05/21/2004
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