BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    SELF-RECORDING ADMITTANCE METER 709

    K Number: K802097 · Decision Oct 10, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    13
    Registration Numbers
    13
    Same Product Code
    69
    Applicant Total
    8
    Review Days
    38

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    Basic Information

    Device Name
    SELF-RECORDING ADMITTANCE METER 709
    K Number
    K802097
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    874.1090
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Applicant
    Amplaid USA, Inc.
    Date Received
    September 2, 1980
    Decision Date
    October 10, 1980
    Product Code
    ETY
    Advisory Committee
    Ear, Nose, Throat
    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
    ETY Tester, Auditory Impedance

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    Other Clearances by Amplaid USA, Inc.

    K Number Device Name
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    K810481 VISUAL PATTERN REVERSAL GEN. & PHOTIC S.
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    K781667 AMPLAID MARK 4 AND MARK 5