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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K161164
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(1) Patient Information Center iX, Model No. 866389 (2) Patient Information Center iX Expand, Model... 2 01/13/2024 Philips North America
(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436 2 01/13/2024 Philips North America
CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Ver... 2 03/27/2024 Philips North America
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