Device Classification Name |
computer, diagnostic, programmable
|
510(k) Number |
K160218 |
Device Name |
AutoMark Module |
Applicant |
St. Jude Medical |
One St. Jude Medical Drive |
St. Paul,
MN
55117
|
|
Applicant Contact |
Melissa Frank |
Correspondent |
St. Jude Medical |
One St. Jude Medical Drive |
St. Paul,
MN
55117
|
|
Correspondent Contact |
Melissa Frank |
Regulation Number | 870.1425
|
Classification Product Code |
|
Date Received | 01/29/2016 |
Decision Date | 12/13/2016 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Cardiovascular
|
510k Review Panel |
Cardiovascular
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
|
|