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FreeStyle Libre 2 Flash Glucose Monitoring System

K211102 Class II Traditional
Decision Date
2021-08-11
Sponsor / Applicant
Abbott Diabetes Care, Inc.

Technical Specification

510(k) Submission ID K211102
Product Code QLG
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1355
Decision Date 2021-08-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FreeStyle Libre 2 Flash Glucose Monitoring System received FDA 510(k) clearance under submission number K211102, sponsored by Abbott Diabetes Care, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2021-08-11.

Classification & Regulation

This clearance is catalogued under FDA product code QLG and 21 CFR 862.1355, within the Clinical Chemistry review panel as a Class II device.