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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
contak renewal tr

supplement #: S047
Guidant Corp. Oct 26, 2007 process change - manufacturer/sterilizer/packager/supplier  
contrak renewal tr

supplement #: S048
Guidant Corp. Dec 05, 2007 process change - manufacturer/sterilizer/packager/supplier  
contak tr 2

supplement #: S049
Guidant Corp. Jan 17, 2008    
contak renewal tr/tr2 family of pacemakers

supplement #: S050
Guidant Corp. Mar 18, 2008 change design/components/specifications/material  
contak renewal tr2

supplement #: S051
Guidant Corp. Apr 03, 2008 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S052
Guidant Corp. Jul 02, 2008 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S053
Guidant Corp. Jul 18, 2008 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S054
Guidant Corp. Sep 26, 2008 process change - manufacturer/sterilizer/packager/supplier  
insignia and contak renewal tr pulse generators

supplement #: S055
Guidant Corp. Jan 23, 2009 change design/components/specifications/material  
contak renewal tr pulse generators

supplement #: S056
Guidant Corp. Mar 11, 2009 process change - manufacturer/sterilizer/packager/supplier  
  We welcome your comments and feedback about Devices@FDA.
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