Device Classification Name |
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
|
510(k) Number |
K123370 |
Device Name |
EZ GLIDE AORTIC CANNULA, AORTIC PERFUSION CANNULA WITH DURAFLO COATING, DISPERSION AORTIC PERFUSION CANNULA |
Applicant |
EDWARDS LIFESCIENCES, LLC. |
12050 Lone Peak Pkwy |
Draper,
UT
84020
|
|
Applicant Contact |
KAREN JONES |
Correspondent |
EDWARDS LIFESCIENCES, LLC. |
12050 Lone Peak Pkwy |
Draper,
UT
84020
|
|
Correspondent Contact |
KAREN JONES |
Regulation Number | 870.4210
|
Classification Product Code |
|
Date Received | 11/01/2012 |
Decision Date | 03/13/2013 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|