Medical Device Manufacturer · US , Cedar Grove , NJ

Respironics New Jersey, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2004

Total

Cleared

Denied

Respironics New Jersey, Inc. has 5 FDA 510(k) cleared medical devices. Based in Cedar Grove, US.

Historical record: 5 cleared submissions from 2004 to 2011. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Respironics New Jersey, Inc.

5 devices

1-5 of 5