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

    CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT

    K Number: K902625 · Decision Oct 26, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    35
    Registration Numbers
    35
    Same Product Code
    32
    Applicant Total
    6
    Review Days
    134

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    Basic Information

    Device Name
    CLINICAL THERMOMETER; RECTAL/ORAL, INNER ARMPIT
    K Number
    K902625
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2920
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Liaoning-Usa Corp.
    Date Received
    June 14, 1990
    Decision Date
    October 26, 1990
    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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