Medical Device Manufacturer · US , Grand Rapids , MI

Medtronic Cardiac Surgical Products - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2000

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

1-7 of 7

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