This page includes the latest FDA filings for Medtronic Cardiac Surgical Products. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
---|---|---|
MEDTRONIC CARDIAC SURGICAL PRODUCTS | MALLEABLE SINGLE STAGE VENOUS CANNULA, MODELS 68112-68140 (15 TOTAL CODES) | 2003-01-08 |
MEDTRONIC CARDIAC SURGICAL PRODUCTS | MEDTRONIC DLP ARTERIAL CANNULA WITH 3D TIP - 22 FR. | 2001-12-04 |
MEDTRONIC CARDIAC SURGICAL PRODUCTS | 24 FR. LEFT HEART VENT CATHETER WITH PRESSURE MONITORING LINE, MODEL 12524 | 2001-10-24 |
MEDTRONIC CARDIAC SURGICAL PRODUCTS | SELECT CAP ARTERIAL CANNULA WITH PRESSURE MONITORING LINE, MODEL 78818,78820,78822,78824,78918,78920,78922,78924 | 2001-04-04 |
MEDTRONIC CARDIAC SURGICAL PRODUCTS | MEDTRONIC DLP ARTERIAL CANNULAE WITH 3D TIP | 2001-02-07 |
MEDTRONIC CARDIAC SURGICAL PRODUCTS | MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE | 2000-04-27 |
MEDTRONIC CARDIAC SURGICAL PRODUCTS | EOPA ELONGATED ONE-PIECE ARTERIAL CANNULA WITH GUIDEWIRE | 2000-02-10 |