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.

Resmed Germany, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

8 devices

1-8 of 8