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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameDELTA(R) PACEMAKER SYSTEM (VIGOR SSI AND DDD MODELS ONLY)
Classification Nameimplantable pulse generator, pacemaker (non-crt)
Generic Namedual chamber, implantable pulse generator
ApplicantGUIDANT CORP.
PMA NumberP840068
Supplement NumberS036
Date Received06/24/1998
Decision Date07/31/1998
Product Code
LWP[ Registered Establishments with LWP ]
Advisory Committee Cardiovascular
Supplement Typereal-time process
Supplement Reason change design/components/specifications - software
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for an update to the model 2881 software application to include the delta/vista pacemakers, series, resulting in version 1. 3 of the model 2881 software application.
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