Device Classification Name |
catheter, percutaneous
|
510(k) Number |
K131592 |
Device Name |
ENLIGHTN RENAL GUIDE CATHETER |
Applicant |
ST. JUDE MEDICAL, INC. |
5050 NATHAN LANE NORTH |
PLYMOUTH,
MN
55442
|
|
Applicant Contact |
BLAIR SCHWARTZ |
Correspondent |
REGULATORY TECHNOLOGY SERVICES, LLC |
1000 Westgate Drive, |
Suite 510k |
Saint Paul,
MN
55114
|
|
Regulation Number | 870.1250
|
Classification Product Code |
|
Date Received | 06/03/2013 |
Decision Date | 01/31/2014 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
Yes
|
Combination Product |
No
|
|
|