BEUDAMED
    FDA PMA FDA Class 2 Approved (Reclassification) 🇺🇸 United States

    Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

    PMA: P840047 · Decision Aug 2, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    3
    Registration Numbers
    4

    Basic Information

    Device Name
    Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla
    Trade Name
    CILCO ND:YAG LASER
    PMA Number
    P840047
    Device Class
    FDA Class 2
    Product Code
    LXS
    Generic Name
    Laser, neodymium:Yag, ophthalmic for posterior capsulotomy and cutting pupilla
    Regulation Number
    886.4392
    Medical Specialty
    Ophthalmic
    Advisory Committee
    Ophthalmic
    Decision
    Approved (Reclassification)
    Decision Code
    APRL
    Decision Date
    August 2, 1985
    Date Received
    October 2, 1984
    Expedited Review
    N
    Docket Number
    85M-0402

    Classifications

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

    Product Code Device Name
    LXS Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla