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

    FEVER METER

    K Number: K821314 · Decision May 28, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    29
    Registration Numbers
    29
    Same Product Code
    20
    Applicant Total
    6
    Review Days
    24

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    Basic Information

    Device Name
    FEVER METER
    K Number
    K821314
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6740
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Steridyne Corp.
    Date Received
    May 4, 1982
    Decision Date
    May 28, 1982
    Product Code
    KDP
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KDP Regulator, Vacuum

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    Other Clearances by Steridyne Corp.

    K Number Device Name
    K925352 CLEAN CUFF BLOOD PRESSURE CUFF LINER
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    K911269 MERCURY AND GLASS FEVER THERMOMETER
    K842120 ZERO-G
    K801458 WINTER HEAD DRESSING