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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameRF CONTACTR CATHETER, RF ENHANCR II CATHETER, RF MARINR CATHETER, RF CONDUCTR CATHETER
Classification Namecardiac ablation percutaneous catheter
Generic Namecardiac ablation system
ApplicantMEDTRONIC, INC.
PMA NumberP930029
Supplement NumberS042
Date Received02/27/2014
Decision Date03/12/2014
Product Code
LPB[ Registered Establishments with LPB ]
Advisory Committee Cardiovascular
Supplement Type30-day notice
Supplement Reason process change: manufacturing
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Use of factoryworks release 7. 10 at several of medtronic¿s manufacturing facilities.
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