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

    TECHNION ELECTRONIC FEVER THERMOMETER

    K Number: K791323 · Decision Sep 7, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    488
    Registration Numbers
    488
    Same Product Code
    797
    Applicant Total
    2
    Review Days
    52

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    Basic Information

    Device Name
    TECHNION ELECTRONIC FEVER THERMOMETER
    K Number
    K791323
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2910
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Technicon Corp.
    Date Received
    July 17, 1979
    Decision Date
    September 7, 1979
    Product Code
    FLL
    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
    FLL Continuous Measurement Thermometer

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    Other Clearances by Technicon Corp.

    K Number Device Name
    K813077 TECHNICON RA 1000 SYSTEM