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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Tester, Pacemaker Electrode Function
510(k) Number K790503
Device Name CARDIOTEST 2200
Applicant
Cardiac Pacemakers, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Cardiac Pacemakers, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.3720
Classification Product Code
DTA  
Date Received03/13/1979
Decision Date 05/17/1979
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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