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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.
 
DeviceDEXCOM SEVEN SYSTEM
Generic NameSensor, glucose, invasive
ApplicantDEXCOM, INC.
5555 OBERLIN DR
SAN DIEGO, CA 92121
PMA NumberP050012
Supplement NumberS016
Date Received08/04/2008
Decision Date02/13/2009
Withdrawal Date 08/28/2015
Product Code MDS 
Advisory Committee Clinical Chemistry
Clinical TrialsNCT00722241
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
APPROVAL FOR MODIFICATIONS TO THE RECEIVER USER INTERFACE AND ALGORITHM, AND MODIFICATIONS TO THE TRANSMITTER TO MAKE IT COMPATIBLE TO THE MODIFIED RECEIVER ALGORITHM.
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