Atlas FDA

Freestyle Libre Flash Glucose Monitoring System

FDA premarket approval P160030/S007 · decided 2018-02-26

Approval details

PMA number
P160030
Supplement
S007
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Freestyle Libre Flash Glucose Monitoring System
Generic name
Sensor, glucose, invasive, non-adjunctive, factory-calibrated, user-initiated
Applicant
Abbott Diabetes Care, Inc.
Date received
2017-12-01
Decision date
2018-02-26
Days to decision
87 days
Decision code
APPR
Product code
PZE
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Alameda, CA
Statement
Approval for design changes to the puck carrier, applicator cap, and container tray of the Freestyle Libre Flash Glucose Monitoring System and Freestyle Libre Pro Flash Glucose Monitoring System, as well as manufacturing changes in increase production capacity for the same components.

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510(k) clearances by this applicant

RecordFirmDate
FreeStyle Libre 3 Continuous Glucose Monitoring System; FreeStyle Libre 2 Flash Glucose Monitoring System (K233537)Abbott Diabetes Care, Inc.2024-04-23
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FreeStyle Libre 2 Flash Glucose Monitoring System; Freestyle Libre 3 Continuous Glucose Monitoring System (K222447)Abbott Diabetes Care, Inc.2023-03-03
FreeStyle Libre 2 System, FreeStyle Libre 3 System (K223537)Abbott Diabetes Care, Inc.2023-02-21
FreeStyle Libre 3 Continuous Glucose Monitoring System (K212132)Abbott Diabetes Care, Inc.2022-05-26
FreeStyle Libre 3 Continuous Glucose Monitoring System (K213996)Abbott Diabetes Care, Inc.2022-05-26
FreeStyle Libre 2 Flash Glucose Monitoring System (with FreeStyle Libre 2 App) (K210943)Abbott Diabetes Care, Inc.2021-11-22
FreeStyle Libre 2 Flash Glucose Monitoring System (K211102)Abbott Diabetes Care, Inc.2021-08-11