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

    BECKMAN DIRECT BILIRUBIN REAGENT

    K Number: K934068 · Decision Apr 26, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    49
    Registration Numbers
    49
    Same Product Code
    234
    Applicant Total
    11
    Review Days
    249

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    Basic Information

    Device Name
    BECKMAN DIRECT BILIRUBIN REAGENT
    K Number
    K934068
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1110
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Beckman-Diagnostic Systems Group
    Date Received
    August 20, 1993
    Decision Date
    April 26, 1994
    Product Code
    CIG
    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
    CIG Diazo Colorimetry, Bilirubin

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