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    FDA PMA FDA Class 3 Approved (Withdrawn) 🇺🇸 United States

    Device. Laser Peripheral Angioplasty

    PMA: P860042 · Decision Feb 27, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0

    Basic Information

    Device Name
    Device. Laser Peripheral Angioplasty
    Trade Name
    TRIMEDYNE'S LASERPROBE-PLR{TM} CATHETER & OPTILASE
    PMA Number
    P860042
    Device Class
    FDA Class 3
    Product Code
    LWX
    Generic Name
    Device. Laser peripheral angioplasty
    Medical Specialty
    Unknown
    Advisory Committee
    Cardiovascular
    Decision
    Approved (Withdrawn)
    Decision Code
    APWD
    Decision Date
    February 27, 1987
    Date Received
    September 2, 1986
    Expedited Review
    N
    Docket Number
    87M-0076

    Classifications

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

    Product Code Device Name
    LWX Device. Laser Peripheral Angioplasty