BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    PANTEX DIRECT ESTRADIOL COATED TUBE RADIOIMMUNOASS

    K Number: K853866 · Decision Oct 15, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    49
    Registration Numbers
    49
    Same Product Code
    49
    Applicant Total
    16
    Review Days
    28

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    Basic Information

    Device Name
    PANTEX DIRECT ESTRADIOL COATED TUBE RADIOIMMUNOASS
    K Number
    K853866
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1260
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Pantex, Div. Bio-Analysis, Inc.
    Date Received
    September 17, 1985
    Decision Date
    October 15, 1985
    Product Code
    CHP
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

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

    Product Code Device Name
    CHP Radioimmunoassay, Estradiol

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