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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.
Classification Namepermanent defibrillator electrodes
Generic Namepermanent defibrillator electrodes
8200 coral sea street ne
ms mv s11
mounds view, MN 55112
PMA NumberP950024
Supplement NumberS048
Date Received04/10/2013
Decision Date12/24/2013
Product Code
NVY[ Registered Establishments with NVY ]
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track no user fee
Supplement Reason location change - manufacturer/sterilizer/packager/supplier
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for a re-packaging/re-labeling site located at medtronic in memphis, tennesee.