PMA
P050012: DEXCOM STS CONTINOUS MONITORS
FDA PMA · Sensor, glucose, invasive · Dexcom, Inc.
Key facts
| PMA number | P050012 |
|---|---|
| Trade name | DEXCOM STS CONTINOUS MONITORS |
| Generic name | Sensor, glucose, invasive |
| Applicant | Dexcom, Inc. |
| Owner/operator | DEXCOM, INC. |
| Product code | MDS |
| Approval date | Mar 24, 2006 |
| Docket number | 06M-0200 |
| Notice date | May 12, 2006 |
| Establishment registration | 3004753838 |
| FEI number | 3004753838 |
At a glance
- 10–99 Supplements
- Mar 5, 2014 Latest supplement decision
- Yes Withdrawn
- Yes Summary of safety and effectiveness on file
- None UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: