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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 family

supplement #: S057
Guidant Corp. May 21, 2009 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S058
Guidant Corp. Nov 16, 2009 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S059
Guidant Corp. Dec 22, 2009 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S060
Guidant Corp. Jan 12, 2010 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr family

supplement #: S061
Guidant Corp. Mar 04, 2010 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S062
Guidant Corp. May 21, 2010 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr family of crt-ps

supplement #: S063
Guidant Corp. May 19, 2010 process change - manufacturer/sterilizer/packager/supplier  
cardiac resynchronization therapy pacemaker (crt-p)

supplement #: S064
Guidant Corp. May 20, 2010 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S065
Guidant Corp. Aug 13, 2010 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S067
Guidant Corp. Apr 08, 2011 process change - manufacturer/sterilizer/packager/supplier  
  We welcome your comments and feedback about Devices@FDA.
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