The device was not returned to olympus medical systems corp.(omsc), but returned to olympus repair center for evaluation.Device history record review indicates that the product was manufactured and tested in accordance with all applicable procedures and met all final product release criteria.The exact cause of the reported event could not be conclusively determined at this time.Omsc surmised that this phenomenon attributed to a failure of the ccd unit, the inner circuit board of connector, or video system center.If additional information becomes available, this report will be supplemented.
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