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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K131982
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Philips DreamStation Auto BiPAP and CPAP, Model Numbers UCDSX500S11, UDSX500S11, UDSX500S11F, UDSX70... 1 04/06/2023 Philips Respironics, Inc.
SystemOne (Q-Series), DreamStation, DreamStation Go, Dorma 400, Dorma 500, REMstar SE Auto Nonconti... 1 07/13/2021 Philips Respironics, Inc.
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