Cardiac Assist, Maquet Cardiovascular, LLC is one of 24536 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiac Assist, Maquet Cardiovascular, LLC - FDA 510(k) Cleared Devic...
Recent clearances: CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP, SENSATION(TM) PLUS 8FR. 50CC INTRA-AORTIC BALLOON CATHETER AND ACCESSORIES
2
Total
2
Cleared
0
Denied
Cardiac Assist, Maquet Cardiovascular, LLC has 2 FDA 510(k) cleared medical devices. Based in Manwah, US.
Historical record: 2 cleared submissions from 2011 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiac Assist, Maquet Cardiovascular, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardiac Assist, Maquet Cardiovascular, LLC
2 devices