FreeStyle Libre 3 Continuous Glucose Monitoring System
K-Number: K212132 · 2022-05-26
Device Summary
Frequently Asked Questions
What is the FreeStyle Libre 3 Continuous Glucose Monitoring System?
FreeStyle Libre 3 Continuous Glucose Monitoring System is a medical device that received FDA 510(k) clearance on 2022-05-26. It is manufactured by Abbott Diabetes Care, Inc.. The 510(k) number is K212132.
When was FreeStyle Libre 3 Continuous Glucose Monitoring System approved by the FDA?
FreeStyle Libre 3 Continuous Glucose Monitoring System received FDA 510(k) clearance on 2022-05-26, under approval number K212132.
What company makes FreeStyle Libre 3 Continuous Glucose Monitoring System?
FreeStyle Libre 3 Continuous Glucose Monitoring System is manufactured by Abbott Diabetes Care, Inc..
What is the FDA product code for FreeStyle Libre 3 Continuous Glucose Monitoring System?
The FDA product code for FreeStyle Libre 3 Continuous Glucose Monitoring System is QLG.
Related Clinical Trials
Related PubMed Literature
Other Devices by Abbott Diabetes Care, Inc.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.