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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original PMA or panel track supplement and may not represent the most recent labeling.
 
DeviceMAESTRO SERIES 500 P.G. MODELS 501, 505, 509
Classification Nameimplantable pulse generator, pacemaker (non-crt)
Generic Nameimplantable pulse generator, pacemaker (non-crt)
Applicant
CARDIAC CONTROL SYSTEMS, INC.
3 commerce blvd.
palm coast, FL 32164
PMA NumberP860027
Date Received07/28/1986
Decision Date02/27/1987
Product Code
LWP[ Registered Establishments with LWP ]
Docket Number 87M-0085
Notice Date 04/16/1987
Advisory Committee Cardiovascular
Expedited Review Granted? No
Combination Product No
Supplements: S001 S002 S003 S004 S005 S006 S007 S008 S009 
S010 S011 S012 
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