Business Wire

Nihon Kohden NKV-330 Ventilator System Receives US FDA 510(k) Clearance

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 ...
Business Wire

ALung Receives IDE Approval to Conduct VENT-AVOID Trial of the Hemolung RAS for the US Market

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 ...