BEUDAMED
    FDA 510(k) Unknown 🇺🇸 United States

    DUPONT ACA LIQUID BILIRUBIN CALIBRATOR

    K Number: K842222 · Decision Jun 5, 1984
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    253
    Review Days
    —

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    Basic Information

    Device Name
    DUPONT ACA LIQUID BILIRUBIN CALIBRATOR
    K Number
    K842222
    Clearance Type
    Traditional
    Decision
    Unknown
    Applicant
    E.I. Dupont DE Nemours & Co., Inc.
    Date Received
    June 5, 1984
    Decision Date
    June 5, 1984
    Advisory Committee
    Unknown
    Review Advisory Committee
    CH
    Third Party
    N

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