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U.S. Department of Health and Human Services

Devices@FDA
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Note: if a medical device has supplements, the device description and instructions may have
changed. Be sure to look at the supplements to get an up-to-date view of this device.
 
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239 supplements returned for P030005

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Device Name Company Date Approved Supplement Reason Other Information
renewal tr

supplement #: S022
Guidant Corp. Aug 06, 2007 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S023
Guidant Corp. Nov 30, 2005 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S024
Guidant Corp. Dec 19, 2005 process change - manufacturer/sterilizer/packager/supplier  
contak renewal cardiac resynchronization therapy pacemaker(crt-p) devices

supplement #: S027
Guidant Corp. Dec 20, 2005 change design/components/specifications/material  
contak renewal tr

supplement #: S028
Guidant Corp. Jan 20, 2006 process change - manufacturer/sterilizer/packager/supplier  
contak renewal

supplement #: S029
Guidant Corp. May 05, 2006 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S030
Guidant Corp. Mar 31, 2006 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S031
Guidant Corp. Mar 31, 2006 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S032
Guidant Corp. Mar 31, 2006 process change - manufacturer/sterilizer/packager/supplier  
renewal tr family of cardiac resynchronization therapy pacemakers

supplement #: S033
Guidant Corp. Apr 26, 2006 process change - manufacturer/sterilizer/packager/supplier  
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