IRVINE, Calif.--(BUSINESS WIRE)--Nihon Kohden OrangeMed, Inc. received U.S. Food and Drug Administration (FDA) 510(k) clearance for its NKV-330 Ventilator System. The NKV-330 is a non-invasive ...
PITTSBURGH--(BUSINESS WIRE)--ALung Technologies, Inc., today announced U.S. Food and Drug Administration (FDA) approval of its Investigational Device Exemption (IDE) to conduct a pivotal clinical ...
Industry stakeholders and patient advocacy groups are raising concerns with CMS due to high denial rates for non-invasive ventilators (NIVs) by Medicare Advantage plans. Industry stakeholders and ...
Global ventilation practices in critically ill pediatric patients vary significantly across age groups and by ARDS status.
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