BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    Kit, Assay, Progesterone Receptor

    PMA: P820052 · Supplement: S005 · Decision Mar 26, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0

    Basic Information

    Device Name
    Kit, Assay, Progesterone Receptor
    Trade Name
    RIANEN(TM) (3H) PROGESTIN RECEPTOR ASSAY KIT
    PMA Number
    P820052
    Supplement Number
    S005
    Device Class
    FDA Class 3
    Product Code
    LPI
    Generic Name
    KIT, ASSAY, PROGESTERONE RECEPTOR
    Regulation Number
    864.1860
    Medical Specialty
    Hematology
    Advisory Committee
    Clinical Chemistry
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    March 26, 1985
    Date Received
    June 15, 1984
    Expedited Review
    N

    Classifications

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

    Product Code Device Name
    LPI Kit, Assay, Progesterone Receptor