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FDA 510(k) Applications for Medical Device Product Code "LQD"
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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 |