This supplemental report is being submitted to provide additional information.The device was not returned to olympus medical systems corp.(omsc), therefore omsc cannot investigate the device.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.According to the evaluation by the olympus field service engineer, the composite cable connected to the non-olympus device had failed.Olympus field service engineer replaced the cable, and the reported phenomenon was solved.If additional information becomes available, this report will be supplemented.
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