510(k) K160210

EnSite Precision Cardiac Mapping System v2.0 by St Jude Medical — Product Code DQK

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 13, 2016
Date Received
January 28, 2016
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Computer, Diagnostic, Programmable
Device Class
Class II
Regulation Number
870.1425
Review Panel
CV
Submission Type