Medtronic Perfusion Systems - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
Medtronic Perfusion Systems has 29 FDA 510(k) cleared cardiovascular devices. Based in Minneapolis, US.
Latest FDA clearance: Jul 2024. Active since 2000.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
29 devices
Cleared
Jul 10, 2024
Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance...
Cardiovascular
124d
Cleared
Aug 22, 2018
autoLog IQ Autotransfusion System
Cardiovascular
30d
Cleared
Mar 19, 2013
AFFINITY AF100 ARTERIAL FILTER WITH CARMEDA BIOACTIVE SURFACE
Cardiovascular
139d
Cleared
Sep 03, 2010
AFFINITY VARD SUB-ASSEMBLY FOR CPS (CARMEDA COATED), PURGELINE (UNCOATED),...
Cardiovascular
128d
Cleared
Aug 27, 2009
MIRCSP (MINIMALLY INVASIVE RETROGRADE CORONARY SINUS PERFUSION) MANUAL...
Cardiovascular
149d
Cleared
May 07, 2008
BIO-CONSOLE 560
Cardiovascular
44d
Cleared
Jun 23, 2006
EOPA 3D ARTERIAL CANNULA, MODELS 78220,78222,78320,783222
Cardiovascular
50d
Cleared
Nov 22, 2005
BIO-MEDICUS MULTI-STAGE VENOUS FEMORAL PERCUTANEOUS KIT
Cardiovascular
69d
Cleared
Sep 22, 2005
MC2X MULTI-STAGE VENOUS CANNULA, MODELS 91437, 91437C
Cardiovascular
23d
Cleared
Jun 10, 2005
BIO-CONSOLE, MODEL 560
Cardiovascular
22d
Cleared
May 24, 2005
HEPARIN DOSE RESPONSE CONTROLS, MODEL 306-20 POR
Hematology
29d
Cleared
Feb 11, 2005
TRILLIUM BIOPUMP PLUS, MODEL BPX80T
Cardiovascular
24d