Upon receipt at our post market quality assurance laboratory, a thorough evaluation of the device was performed.A visual inspection of the device header and case noted no anomalies.Reviewed of device memory confirmed two low voltage codes due to the device being exposed to cold temperatures.The device was then exposed to simulated heart load conditions, and the right ventricular pacing, and sensing functions were tested.The device operated appropriately with no interruptions in therapy output at the returned programmed settings.
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