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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 PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceSEVEN SYSTEM
Generic NameSensor, glucose, invasive
ApplicantDEXCOM, INC.
5555 OBERLIN DR
SAN DIEGO, CA 92121
PMA NumberP050012
Supplement NumberS014
Date Received04/01/2008
Decision Date05/15/2008
Withdrawal Date 08/28/2015
Product Code MDS 
Advisory Committee Clinical Chemistry
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
APPROVAL FOR A DESIGN MODIFICATION TO ALLOW USERS OF THE DEXCOM SEVEN SYSTEM DM2 DATA MANAGER SOFTWARE TO OBTAIN RECEIVER FIRMWARE UPDATES ELECTRONICALLY AND REMOTELY USING THEIR PERSONAL COMPUTER.
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