BEUDAMED
    FDA PMA FDA Class 3 Approved (Withdrawn) 🇺🇸 United States

    Hepatitis Delta Serological Reagents

    PMA: P850062 · Decision Jul 1, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2

    Basic Information

    Device Name
    Hepatitis Delta Serological Reagents
    Trade Name
    ABBOTT ANTI-DELTA DIAGNOSTIC KIT (RIA)
    PMA Number
    P850062
    Device Class
    FDA Class 3
    Product Code
    LQI
    Generic Name
    HEPATITIS DELTA SEROLOGICAL REAGENTS
    Medical Specialty
    Unknown
    Advisory Committee
    Microbiology
    Decision
    Approved (Withdrawn)
    Decision Code
    APWD
    Decision Date
    July 1, 1986
    Date Received
    August 29, 1985
    Expedited Review
    N
    Docket Number
    86M-0308

    Classifications

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

    Product Code Device Name
    LQI Hepatitis Delta Serological Reagents