BEUDAMED
    FDA PMA FDA Class 2 Approved 🇺🇸 United States

    System, Test, Carcinoembryonic Antigen

    PMA: P800063 · Supplement: S004 · Decision Oct 18, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    30
    Registration Numbers
    30

    Basic Information

    Device Name
    System, Test, Carcinoembryonic Antigen
    Trade Name
    CEA-ROCHE TEST KIT
    PMA Number
    P800063
    Supplement Number
    S004
    Device Class
    FDA Class 2
    Product Code
    DHX
    Generic Name
    SYSTEM, TEST, CARCINOEMBRYONIC ANTIGEN
    Regulation Number
    866.6010
    Medical Specialty
    Immunology
    Advisory Committee
    Immunology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    October 18, 1983
    Date Received
    December 15, 1982
    Expedited Review
    N

    Classifications

    This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    DHX System, Test, Carcinoembryonic Antigen