BEUDAMED
    FDA PMA FDA Class 3 Approved 🇺🇸 United States

    System, Rf/Microwave Hyperthermia, Cancer Treatment

    PMA: P820088 · Supplement: S002 · Decision Jul 24, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    1
    Registration Numbers
    1

    Basic Information

    Device Name
    System, Rf/Microwave Hyperthermia, Cancer Treatment
    Trade Name
    BSD 1000 HYPERTHERMIA SYSTEM
    PMA Number
    P820088
    Supplement Number
    S002
    Device Class
    FDA Class 3
    Product Code
    LOC
    Generic Name
    System, rf/microwave hyperthermia, cancer treatment
    Medical Specialty
    Unknown
    Advisory Committee
    Radiology
    Decision
    Approved
    Decision Code
    APPR
    Decision Date
    July 24, 1984
    Date Received
    November 28, 1983
    Supplement Type
    Normal 180 Day Track
    Expedited Review
    N

    Classifications

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

    Product Code Device Name
    LOC System, Rf/Microwave Hyperthermia, Cancer Treatment