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The FDA is committed to using every tool at our disposal to increase the schedule of these clinical products. The FDA is collaborating with Philips Respironics to keep track of the repair service or substitute of impacted devices as expeditiously as possible and also is continuing to collect details to educate our actions. We are collaborating with various other manufacturers and government partners to support schedule of CPAP as well as BiPAP devices. People with details forms of sleep apnea, COPD, obesity-hypoventilation syndrome, and neurological conditions that affect breathing, such as ALS, must use BiPAP devices. https://hub.docker.com/r/morganmjgc/website |
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