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

    GEON DIGITAL CLINICAL THERMOMETER

    K Number: K003223 · Decision Jan 12, 2001
    View on FDA
    Classifications
    1
    FEI Numbers
    488
    Registration Numbers
    488
    Same Product Code
    797
    Applicant Total
    2
    Review Days
    88

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    Basic Information

    Device Name
    GEON DIGITAL CLINICAL THERMOMETER
    K Number
    K003223
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2910
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Geon Corp.
    Date Received
    October 16, 2000
    Decision Date
    January 12, 2001
    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 Geon Corp.

    K Number Device Name
    K952001 GEON ELECTRONIC THERMOMETER