The following data is part of a premarket notification filed by Abbott Diabetes Care, Inc. with the FDA for Freestyle Libre 2 Flash Glucose Monitoring System.
| Device ID | K211102 |
| 510k Number | K211102 |
| Device Name: | FreeStyle Libre 2 Flash Glucose Monitoring System |
| Classification | Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery Systems |
| Applicant | Abbott Diabetes Care, Inc. 1360 South Loop Road Alameda, CA 94502 |
| Contact | Catherine Yang |
| Correspondent | Catherine Yang Abbott Diabetes Care, Inc. 1360 South Loop Road Alameda, CA 94502 |
| Product Code | QLG |
| CFR Regulation Number | 862.1355 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-04-13 |
| Decision Date | 2021-08-11 |