Nihon Kohden Orangemed, Inc.

Nihon Kohden Orangemed, Inc. — FDA 510(k) Submissions

Nihon Kohden Orangemed, Inc. has submitted 4 FDA 510(k) premarket notifications since 2018, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ventilator, Continuous, Facility Use, Ventilator, Continuous, Minimal Ventilatory Support, Facility Use . Use the specialty filter in the sidebar to narrow results.