The device was returned to philips for evaluation.Due to a change in decontamination processes which also involved a facility change, the device cannot be located.Due to age of the complaint, the case will be closed.If/when the device be located, evaluation of the device will be documented in the defoa database under (b)(4).The customer was sent a replacement device.Reference manufacturer's report number 1218950-2020-04914 sent with incorrect registration number.Reference manufacturer's report number 1218950-2020-04914 previously submitted with incorrect registration number.
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