BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    VIBROTACTILE TESTER, MODEL NO. VTT-100

    K Number: K921560 · Decision Oct 30, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    7
    Registration Numbers
    7
    Same Product Code
    12
    Applicant Total
    1
    Review Days
    212

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    Basic Information

    Device Name
    VIBROTACTILE TESTER, MODEL NO. VTT-100
    K Number
    K921560
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    882.1200
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Topical Testing, Inc.
    Date Received
    April 1, 1992
    Decision Date
    October 30, 1992
    Product Code
    LLN
    Advisory Committee
    Neurology
    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
    LLN Device, Vibration Threshold Measurement

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