BEUDAMED
    FDA Adverse Event Summary report: N

    VITAL

    MDR report key: 24948 · Received August 25, 1995

    Report

    Report Number
    MW4000694
    Date Received
    August 25, 1995
    Report Date
    April 6, 1995
    Manufacturer
    ESION CORP.
    Product Code
    MBQ
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    DIETICIAN

    Narratives

    Description of Event or Problem · 1

    COMPLAINT ABOUT THE DEVICE BEING USED ON CHILDREN TO DIAGNOSE FOOD ALLERGIES. DEVICE SUPPOSEDLY COMPARES ELECTROMAGNETIC FIELD OF THE BODY TO THE ELECTROMAGNETIC FIELD OF WHATEVER YOU ARE COMPARING IT TO. DR SAYS SHE USES AS A SCANNING DEVICE. SHE ALSO SAYS THE CO IS OUT OF BUSINESS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VITAL VITAL MBQ ESION CORP. 623

    Patients

    Seq Age Sex Outcome Treatment
    1 *