| 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. |
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| Device | SEVEN SYSTEM |
| Generic Name | Sensor, glucose, invasive |
| Applicant | Dexcom, Inc. 5555 Oberlin Dr. San Diego, CA 92121 |
| PMA Number | P050012 |
| Supplement Number | S014 |
| Date Received | 04/01/2008 |
| Decision Date | 05/15/2008 |
| Withdrawal Date | 08/28/2015 |
| Product Code |
MDS |
| Advisory Committee |
Clinical Chemistry |
| Supplement Type | Real-Time Process |
| Supplement Reason | Change Design/Components/Specifications/Material |
| Expedited Review Granted? | No |
| Combination Product | No |
| Predetermined Change Control Plan Authorized | No |
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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