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

    EQUITEST

    K Number: K851744 · Decision Aug 5, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    21
    Applicant Total
    5
    Review Days
    98

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    Basic Information

    Device Name
    EQUITEST
    K Number
    K851744
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Neurocom International, Inc.
    Date Received
    April 29, 1985
    Decision Date
    August 5, 1985
    Product Code
    LXV
    Advisory Committee
    Unknown
    Review Advisory Committee
    EN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LXV Apparatus, Vestibular Analysis

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    Other Clearances by Neurocom International, Inc.

    K Number Device Name
    K946229 BALANCE MANAGER
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    K871652 NEUROCOM PRESSURE TEST SYSTEM
    K863443 DUAL FORCEPLATE