FDA 510(k) Application Details - K960732

Device Classification Name	Electrode, Cutaneous   More FDA Info for this Device
510(K) Number	K960732
Device Name	Electrode, Cutaneous
Applicant	PHYSIOMETRIX, INC. 101 BILLERICA AVE., BLDG. 5 N. BILLERICA, MA 01862 US Other 510(k) Applications for this Company
Contact	DAWN E FRAZER 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	02/22/1996
Decision Date	04/15/1996
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