Maquet Cardiopulmonary, AG is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Maquet Cardiopulmonary, AG - FDA 510(k) Cleared Devices
44
Total
44
Cleared
0
Denied
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.
Maquet Cardiopulmonary, AG — FDA 510(k) Products and Clearance History
44 devices
Cleared
May 07, 2015
QUADROX-i Adult/Small Adult Oxygenators
Cardiovascular
92d
Cleared
Nov 19, 2014
ANTEGRADE CARDIOPLEGIA CANNULA(N-TYPE)
Cardiovascular
258d
Cleared
Jul 07, 2014
NEONATAL VENOUS HARDSHELL CARDIOTOMY RESERVIOR, PEDIATRIC VENOUS HARDSHELL...
Cardiovascular
38d
Cleared
May 21, 2014
CARDIOHELP SYSTEM
Cardiovascular
180d
Cleared
Nov 12, 2013
QUADROX-IR ADULT AND SMALL ADULT
Cardiovascular
20d
Cleared
Oct 30, 2013
VENOUS HARDSHELL CARDIOTOMY RESERVOIR
Cardiovascular
110d
Cleared
Oct 08, 2013
QUADROX-I, QUADROX-ID, QUADROX-IR OXYGENATORS
Cardiovascular
29d
Cleared
Jul 05, 2013
ARTERIAL HLS CANNULA 13 FR NON-COATED, WITH BIOLINE COATING AND WITH SOFTLINE...
Cardiovascular
28d
Cleared
Jul 01, 2013
HEATER-COOLER UNIT HCU 40
Cardiovascular
144d
Cleared
Jun 26, 2013
HEMOCONCENTRATOR
Gastroenterology & Urology
247d
Cleared
May 16, 2013
ELITE-I (BI) DUAL LUMEN CATHETER
Cardiovascular
66d
Cleared
Sep 15, 2011
QUADROX-I MICROPORPOROUS MEMBRANE OXGENATOR SERIES AND QUDROX-ID DIFFUSION...
Cardiovascular
29d
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