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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Wire, Guide, Catheter
510(k) Number K120298
FOIA Releasable 510(k) K120298
Device Name CPS EXCEL MEDIGUIDE ENABLED GUIDEWIRE
Applicant
ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI
15900 VALLEY VIEW CT.
SYLMAR,  CA  91342
Applicant Contact COLLEEN CANAN
Correspondent
ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI
15900 VALLEY VIEW CT.
SYLMAR,  CA  91342
Correspondent Contact COLLEEN CANAN
Regulation Number870.1330
Classification Product Code
DQX  
Date Received01/31/2012
Decision Date 05/08/2012
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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