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    FDA PMA FDA Class 3 Approved (Withdrawn) 🇺🇸 United States

    Applicator, Hyperthermia, Interstitial

    PMA: P880078 · Decision Oct 17, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    1
    Registration Numbers
    1

    Basic Information

    Device Name
    Applicator, Hyperthermia, Interstitial
    Trade Name
    VH8500 HYPERTHERMIA TREATMENT SYSTEM
    PMA Number
    P880078
    Device Class
    FDA Class 3
    Product Code
    LMZ
    Generic Name
    Applicator, hyperthermia, interstitial
    Medical Specialty
    Unknown
    Advisory Committee
    Radiology
    Decision
    Approved (Withdrawn)
    Decision Code
    APWD
    Decision Date
    October 17, 1989
    Date Received
    October 31, 1988
    Expedited Review
    N
    Docket Number
    89M-0461

    Classifications

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

    Product Code Device Name
    LMZ Applicator, Hyperthermia, Interstitial