FDA 510(k) Application Details - K102614

Device Classification Name	Electrode, Cutaneous   More FDA Info for this Device
510(K) Number	K102614
Device Name	Electrode, Cutaneous
Applicant	BIO-MEDICAL RESEARCH, LTD. BMR HOUSE PARKMORE BUSINESS PARK, WEST GALWAY EI IE Other 510(k) Applications for this Company
Contact	ANNE-MARIE KEENAN 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	09/10/2010
Decision Date	06/03/2011
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