FDA 510(k) Applications for Medical Device Product Code "LQD"
(Recorder, Attention Task Performance)

FDA 510(k) Number Applicant Device Name Decision Date
K141865 ANTHROTRONIX, INC DANA 10/15/2014
K020800 OPTAX SYSTEMS, INC. OPTAX SYSTEM 06/10/2002
K133382 QBTECH AB QB TEST 03/24/2014
K143468 QBTECH AB QbCheck 03/22/2016
K122149 QBTECH AB QBTES 10/17/2012
K040894 QBTECH AB QBTEST 06/22/2004
K173915 The TOVA Company Test of Variables of Attention (T.O.V.A.) 03/22/2018
K170082 THE TOVA COMPANY Test of Variables of Attention (T.O.V.A.) Version 9.0 05/17/2017


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