Medical Device Manufacturer · AU , Bella Vista

Resmed Pty , Ltd.

3 submissions · 3 cleared · Since 2020
3
Total
3
Cleared
0
Denied

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.

3 devices
1–3 of 3
Filters
All3 Anesthesiology 3