BEUDAMED
    FDA Adverse Event Other Summary report: N

    1221842-2002-00001

    MDR report key: 431155 · Received November 4, 2002

    Report

    Report Number
    1221842-2002-00001
    Event Type
    Other
    Date Received
    November 4, 2002
    Date of Event
    May 9, 2000
    Report Date
    November 4, 2002
    Manufacturer
    VISX, INC
    Product Code
    LZS
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LZS VISX, INC

    Patients

    Seq Age Sex Outcome Treatment
    1