Medical Device Manufacturer · US , Brea , CA

Beckman Coulter Ireland, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2013

Total

Cleared

Denied

Beckman Coulter Ireland, Inc. has 7 FDA 510(k) cleared medical devices. Based in Brea, US.

Historical record: 7 cleared submissions from 2013 to 2019. Primary specialty: Chemistry.

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

FDA 510(k) cleared devices by Beckman Coulter Ireland, Inc.

7 devices

1-7 of 7