| 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. |
| |
| Device | DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM |
| Generic Name | Sensor, glucose, invasive |
| Applicant | Dexcom, Inc. 6340 Sequence Dr. San Diego, CA 92121 |
| PMA Number | P120005 |
| Supplement Number | S004 |
| Date Received | 03/11/2013 |
| Decision Date | 04/11/2013 |
| Withdrawal Date | 03/20/2026 |
| Product Code |
MDS |
| Advisory Committee |
Clinical Chemistry |
| Clinical Trials | NCT01514292
|
| Supplement Type | 30-Day Notice |
| Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Expedited Review Granted? | No |
| Combination Product | No |
| Predetermined Change Control Plan Authorized | No |
| Recalls | CDRH Recalls |
Approval Order Statement MANUFACTURING PROCESS CHANGE TO THE AUTOMATED FLUIDICS DIPPER SENSOR FOR THE RESISTANCE MEMBRANE LAYER OF THE G4 PLATINUM SENSOR. |
|
|