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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
510(k) Number K880936
Device Name TRIAD-EP
Applicant
Cardiotronics, Inc.
2726 Loker Ave.
West Carlsbad,  CA  92008
Applicant Contact TIM J WAY
Correspondent
Cardiotronics, Inc.
2726 Loker Ave.
West Carlsbad,  CA  92008
Correspondent Contact TIM J WAY
Regulation Number870.5550
Classification Product Code
DRO  
Date Received03/07/1988
Decision Date 07/18/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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