FDA 510(k) Applications Submitted by MEDTRONIC CARDIAC SURGICAL PRODUCTS
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K000274 |
01/31/2000 |
EOPA ELONGATED ONE-PIECE ARTERIAL CANNULA WITH GUIDEWIRE |
MEDTRONIC CARDIAC SURGICAL PRODUCTS |
| K000776 |
03/10/2000 |
MEDTRONIC DLP ARTERIAL CANNULAE WITH 3D TIP |
MEDTRONIC CARDIAC SURGICAL PRODUCTS |
| K994171 |
12/10/1999 |
MEDTRONIC AORTOCORONARY SHUNT AND SEPARATELY PACKAGED ARTERIOTOMY CANNULAE |
MEDTRONIC CARDIAC SURGICAL PRODUCTS |
| K010737 |
03/12/2001 |
SELECT CAP ARTERIAL CANNULA WITH PRESSURE MONITORING LINE, MODEL 78818,78820,78822,78824,78918,78920,78922,78924 |
MEDTRONIC CARDIAC SURGICAL PRODUCTS |
| K012143 |
07/10/2001 |
24 FR. LEFT HEART VENT CATHETER WITH PRESSURE MONITORING LINE, MODEL 12524 |
MEDTRONIC CARDIAC SURGICAL PRODUCTS |
| K022272 |
07/15/2002 |
MALLEABLE SINGLE STAGE VENOUS CANNULA, MODELS 68112-68140 (15 TOTAL CODES) |
MEDTRONIC CARDIAC SURGICAL PRODUCTS |
| K013013 |
09/07/2001 |
MEDTRONIC DLP ARTERIAL CANNULA WITH 3D TIP - 22 FR. |
MEDTRONIC CARDIAC SURGICAL PRODUCTS |
|
|
