FDA 510(k) Application Details - K980229

Device Classification Name	Electrode, Cutaneous   More FDA Info for this Device
510(K) Number	K980229
Device Name	Electrode, Cutaneous
Applicant	MSB LTD. HILLDROP LANE, RAMSBURY MARLBOROUGH, WILTSHIRE SN8 2RB GB Other 510(k) Applications for this Company
Contact	PETER MARKS 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	01/22/1998
Decision Date	02/27/1998
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