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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K113053
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Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructiv... 1 09/09/2022 Philips Respironics, Inc.
A-Series BiPAP Hybrid A30 (not marketed in US), A-Series BiPAP V30 Auto Continuous Ventilator, Minim... 1 07/15/2021 Philips Respironics, Inc.
A-Series BiPAP A 40, A-Series BiPAP A30 Continuous Ventilator, Non-life Supporting 1 07/15/2021 Philips Respironics, Inc.
DreamStation ASV, DreamStation ST, AVAPS, SystemOne ASV4, C-Series ASV, C-Series S/T and AVAPS, Omni... 1 07/13/2021 Philips Respironics, Inc.
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