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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Computer, Diagnostic, Programmable
510(k) Number K171583
Device Name RhythmView Workstation
Applicant
Abbott Electrophysiology
1530 Obrien Drive, Suite B
Menlo Park,  CA  94025
Applicant Contact Dennis Pozzo
Correspondent
Abbott Electrophysiology
3668 S. Geyer Road, Suite 365
St. Louis,  MO  63127
Correspondent Contact Dennis Pozzo
Regulation Number870.1425
Classification Product Code
DQK  
Date Received05/31/2017
Decision Date 09/01/2017
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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