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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 #: S011
Guidant Corp. Sep 09, 2005 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S012
Guidant Corp. Sep 07, 2005 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr is-1 family

supplement #: S013
Guidant Corp. Sep 07, 2005 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr models h120 and h125

supplement #: S014
Guidant Corp. Sep 13, 2005 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr models h120 and h125

supplement #: S015
Guidant Corp. Sep 08, 2005 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S016
Guidant Corp. Sep 13, 2005    
contak renewal tr

supplement #: S018
Guidant Corp. Sep 27, 2005 process change - manufacturer/sterilizer/packager/supplier  
contak renwal tr2

supplement #: S019
Guidant Corp. Jun 28, 2006 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S020
Guidant Corp. Oct 12, 2005 process change - manufacturer/sterilizer/packager/supplier  
contak renewal tr

supplement #: S021
Guidant Corp. Dec 21, 2005 process change - manufacturer/sterilizer/packager/supplier  
  We welcome your comments and feedback about Devices@FDA.
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