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    FDA PMA FDA Class 3 Approved (Withdrawn) 🇺🇸 United States

    Device, Testicular Hypothermia

    PMA: P820034 · Decision Dec 26, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0

    Basic Information

    Device Name
    Device, Testicular Hypothermia
    Trade Name
    REPRO-MED - THD
    PMA Number
    P820034
    Device Class
    FDA Class 3
    Product Code
    LOA
    Generic Name
    DEVICE, TESTICULAR HYPOTHERMIA
    Medical Specialty
    Unknown
    Advisory Committee
    Gastroenterology, Urology
    Decision
    Approved (Withdrawn)
    Decision Code
    APWD
    Decision Date
    December 26, 1984
    Date Received
    May 28, 1982
    Expedited Review
    N
    Docket Number
    85M-0007

    Classifications

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

    Product Code Device Name
    LOA Device, Testicular Hypothermia