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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 NameRENEWAL 3 RF CONTAK & RENEWAL PG, LIVIAN CRT-D
Classification Nameimplantable pulse generator, pacemaker (non-crt)
Generic Namepulse generator
ApplicantGUIDANT CORP.
PMA NumberP010012
Supplement NumberS166
Date Received12/11/2007
Decision Date01/30/2008
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 the latitude communicator software (model 6482) version 2. 1 and related system software (model 6488) that contains regulated application server (ras) software version 2. 40 as well as associated labeling and operator manual updates. The software modifications are intended to support new device models (livian), make minor software corrections, and improve ease of use with the latitude system.
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