FDA 510(k) Application Details - K170082

Device Classification Name	Recorder, Attention Task Performance   More FDA Info for this Device
510(K) Number	K170082
Device Name	Recorder, Attention Task Performance
Applicant	THE TOVA COMPANY 2828 SW CORBETT AVE SUITE 128 PORTLAND, OR 97201 US Other 510(k) Applications for this Company
Contact	CHRIS HOLDER Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LQD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/10/2017
Decision Date	05/17/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review