Medtronic Cardiac Surgical Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtronic Cardiac Surgical Products - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Medtronic Cardiac Surgical Products has 7 FDA 510(k) cleared medical devices. Based in Grand Rapids, US.
Historical record: 7 cleared submissions from 2000 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medtronic Cardiac Surgical Products Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medtronic Cardiac Surgical Products
7 devices
Cleared
Jan 08, 2003
MALLEABLE SINGLE STAGE VENOUS CANNULA, MODELS 68112-68140 (15 TOTAL CODES)
Cardiovascular
177d
Cleared
Dec 04, 2001
MEDTRONIC DLP ARTERIAL CANNULA WITH 3D TIP - 22 FR.
Cardiovascular
88d
Cleared
Oct 24, 2001
24 FR. LEFT HEART VENT CATHETER WITH PRESSURE MONITORING LINE, MODEL 12524
Cardiovascular
106d
Cleared
Apr 04, 2001
SELECT CAP ARTERIAL CANNULA WITH PRESSURE MONITORING LINE, MODEL...
Cardiovascular
23d
Cleared
Feb 07, 2001
MEDTRONIC DLP ARTERIAL CANNULAE WITH 3D TIP
Cardiovascular
334d
Cleared
Apr 27, 2000
MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE
Cardiovascular
139d
Cleared
Feb 10, 2000
EOPA ELONGATED ONE-PIECE ARTERIAL CANNULA WITH GUIDEWIRE
Cardiovascular
10d