FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App)
K-Number: K201761 · 2021-07-30
Device Summary
Frequently Asked Questions
What is the FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App)?
FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App) is a medical device that received FDA 510(k) clearance on 2021-07-30. It is manufactured by Abbott Diabetes Care, Inc.. The 510(k) number is K201761.
When was FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App) approved by the FDA?
FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App) received FDA 510(k) clearance on 2021-07-30, under approval number K201761.
What company makes FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App)?
FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App) is manufactured by Abbott Diabetes Care, Inc..
What is the FDA product code for FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App)?
The FDA product code for FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App) is QLG.
Related Clinical Trials
Related PubMed Literature
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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.