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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Implantable Pacemaker Pulse-Generator
510(k) Number K880422
Device Name MAESTRO(R) MODEL 119, SINGLE-CHAMBER PACEMAKER
Applicant
CARDIAC CONTROL SYSTEMS, INC.
3 COMMERCE BLVD.
PALM COAST,  FL  32164
Applicant Contact Scott J Mindrebo
Correspondent
CARDIAC CONTROL SYSTEMS, INC.
3 COMMERCE BLVD.
PALM COAST,  FL  32164
Correspondent Contact Scott J Mindrebo
Regulation Number870.3610
Classification Product Code
DXY  
Date Received02/01/1988
Decision Date 03/31/1988
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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