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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K090539
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OmniLab Advanced + Ventilator Product Numbers 1111122 1111123 1111124 1111125 1111126 1111127 1... 1 05/23/2024 Philips Respironics, Inc.
Philips OmniLab Advanced+ Intl (Flow Gen), Rx Only. To provide noninvasive ventilation support for ... 1 09/09/2022 Philips Respironics, Inc.
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