FDA 510(k) Application Details - K080217

Device Classification Name	Amplitude-Integrated Electroencephalograph   More FDA Info for this Device
510(K) Number	K080217
Device Name	Amplitude-Integrated Electroencephalograph
Applicant	MOBERG RESEARCH, INC. 224 S. MAPLE WAY AMBLER, PA 19002 US Other 510(k) Applications for this Company
Contact	Damon Lees Other 510(k) Applications for this Contact
Regulation Number	882.1400   More FDA Info for this Regulation Number
Classification Product Code	OMA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/29/2008
Decision Date	11/05/2008
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	Y
Expedited Review