BEUDAMED
    FDA Adverse Event Summary report: N

    1933441-1997-00004

    MDR report key: 102998 · Received June 30, 1997

    Report

    Report Number
    1933441-1997-00004
    Date Received
    June 30, 1997
    Date of Event
    May 4, 1997
    Product Code
    FSA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FSA

    Patients

    Seq Age Sex Outcome Treatment
    1