BEUDAMED
    FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

    Alfapump System

    PMA: P230044 · Supplement: S004 · Decision May 5, 2026
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0

    Basic Information

    Device Name
    Alfapump System
    Trade Name
    alfapump System
    PMA Number
    P230044
    Supplement Number
    S004
    Device Class
    FDA Class 3
    Product Code
    SDQ
    Generic Name
    alfapump System
    Medical Specialty
    Unknown
    Advisory Committee
    Gastroenterology, Urology
    Decision
    30-Day Notice Accepted
    Decision Code
    OK30
    Decision Date
    May 5, 2026
    Date Received
    April 10, 2026
    Supplement Type
    30-Day Notice
    Supplement Reason
    Process Change - Manufacturer/Sterilizer/Packager/Supplier
    Expedited Review
    N

    Advisory Committee Statement

    Approval for change to the equipment used for solder mask exposure during manufacturing of a printed circuit board.

    Classifications

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

    Product Code Device Name
    SDQ Alfapump System