Medical Device Manufacturer · US , Poway , CA

Resmed Germany, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2006

Total

Cleared

Denied

Resmed Germany, Inc. has 8 FDA 510(k) cleared medical devices. Based in Poway, US.

Historical record: 8 cleared submissions from 2006 to 2015. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Resmed Germany, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Resmed Germany, Inc.

8 devices

1-8 of 8