Medical Device Manufacturer · US , Grand Rapids , MI

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

7 submissions · 7 cleared · Since 2000

Recent clearances: MALLEABLE SINGLE STAGE VENOUS CANNULA, MODELS 68112-68140 (15 TOTAL CODES), MEDTRONIC DLP ARTERIAL CANNULA WITH 3D TIP - 22 FR., 24 FR. LEFT HEART VENT CATHETER WITH PRESSURE MONITORING LINE, MODEL 12524

View 7 510(k) 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.

Medtronic Cardiac Surgical Products is one of 26042 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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