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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 NameVIGOR MODEL 2880 SOFTWARE APPLICATION
Classification Nameimplantable pulse generator, pacemaker (non-crt)
Generic Namedual chamber, implantable pulse generator
ApplicantGUIDANT CORP.
PMA NumberP840068
Supplement NumberS028
Date Received09/11/1995
Decision Date03/22/1996
Product Code
LWP[ Registered Establishments with LWP ]
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - software
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the use of the vigor model 2880 software application used in conjunction with the model 2909 multiple application utility (mau) on the model 2950 prm for programming of all commercially available vigor pacemakers.
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