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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
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