FDA 510(k) Application Details - K020445

Device Classification Name	Electrode, Cutaneous   More FDA Info for this Device
510(K) Number	K020445
Device Name	Electrode, Cutaneous
Applicant	THE ELECTRODE STORE, INC. 936-11TH AVENUE EAST SEATTLE, WA 98102 US Other 510(k) Applications for this Company
Contact	CARL YOUNGMANN Other 510(k) Applications for this Contact
Regulation Number	882.1320   More FDA Info for this Regulation Number
Classification Product Code	GXY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/11/2002
Decision Date	05/10/2002
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