FDA 510(k) Application Details - K990370

Device Classification Name	Electrode, Cutaneous   More FDA Info for this Device
510(K) Number	K990370
Device Name	Electrode, Cutaneous
Applicant	MSB,UK BROOKSIDE COTTAGE,RAMSBURY MARLBOROUGH,WILTSHIRE GB Other 510(k) Applications for this Company
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	02/08/1999
Decision Date	04/12/1999
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