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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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438 supplements returned for P860004

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Device Name Company Date Approved Supplement Reason Other Information
synchromed infusion system

supplement #: S225
Medtronic, Inc. Apr 02, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S226
Medtronic, Inc. Apr 17, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S227
Medtronic, Inc. May 18, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S228
Medtronic, Inc. Jun 26, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S229
Medtronic, Inc. Jun 26, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed drug infusion system

supplement #: S230
Medtronic, Inc. Jul 01, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S231
Medtronic, Inc. Jul 16, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S232
Medtronic, Inc. Jul 16, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S234
Medtronic, Inc. Aug 18, 2015 process change - manufacturer/sterilizer/packager/supplier  
synchromed infusion system

supplement #: S235
Medtronic, Inc. Dec 30, 2015 process change - manufacturer/sterilizer/packager/supplier  
  We welcome your comments and feedback about Devices@FDA.
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