BEUDAMED
    FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

    Test of Variables of Attention (T.O.V.A.)

    K Number: K173915 · Decision Mar 22, 2018
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    10
    Applicant Total
    2
    Review Days
    90

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    Basic Information

    Device Name
    Test of Variables of Attention (T.O.V.A.)
    K Number
    K173915
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    The Tova Company
    Date Received
    December 22, 2017
    Decision Date
    March 22, 2018
    Product Code
    LQD
    Advisory Committee
    Unknown
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LQD Recorder, Attention Task Performance

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (LQD), ordered by most recent decision date.

    Test of Variables of Attention (T.O.V.A.) Version 9.0

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    Other Clearances by The Tova Company

    K Number Device Name
    K170082 Test of Variables of Attention (T.O.V.A.) Version 9.0