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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K113053
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A-Series BiPAP Hybrid A30 (not marketed in US), A-Series BiPAP V30 Auto Continuous Ventilator, Minim... 1 07/15/2021 FEI # 2518422
Philips Respironics, Inc.
Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructiv... 1 09/09/2022 FEI # 2518422
Philips Respironics, Inc.
BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support in adult and pediatric pa... 1 07/02/2025 FEI # 2518422
Philips Respironics, Inc.
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