Maquet Cardiopulmonary, AG - FDA 510(k) Cleared Devices

Maquet Cardiopulmonary, AG has 44 FDA 510(k) cleared cardiovascular devices. Based in Fairfield, US.

Historical record: 44 cleared submissions from 2005 to 2015.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Intertek Testing Services and Maquet Cardiovascular.