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

    THERMOMETER, MERCURY/CLINICAL

    K Number: K883573 · Decision Nov 7, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    35
    Registration Numbers
    35
    Same Product Code
    32
    Applicant Total
    1
    Review Days
    77

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    Basic Information

    Device Name
    THERMOMETER, MERCURY/CLINICAL
    K Number
    K883573
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2920
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Umax Corp.
    Date Received
    August 22, 1988
    Decision Date
    November 7, 1988
    Product Code
    FLK
    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
    FLK Thermometer, Clinical Mercury

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