Resmed Pty , Ltd.

Resmed Pty , Ltd. — FDA 510(k) Submissions

Resmed Pty , Ltd. has submitted 3 FDA 510(k) premarket notifications since 2020, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ventilator, Non-continuous (respirator), Ventilator, Continuous, Non-life-supporting . Use the specialty filter in the sidebar to narrow results.