FDA 510(k) Application Details - K141883

Device Classification Name	Automatic Event Detection Software For Full-Montage Electroencephalograph   More FDA Info for this Device
510(K) Number	K141883
Device Name	Automatic Event Detection Software For Full-Montage Electroencephalograph
Applicant	PICOFEMTO LLC 131 W. 35TH STREET, 8TH FLOOR NEW YORK, NY 10001 US Other 510(k) Applications for this Company
Contact	SRIKANT KRISHNA Other 510(k) Applications for this Contact
Regulation Number	882.1400   More FDA Info for this Regulation Number
Classification Product Code	OMB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/11/2014
Decision Date	05/15/2015
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