Atlas FDA

Freestyle Libre Pro Flash Glucose Monitoring System

FDA premarket approval P150021/S038 · decided 2019-03-19

Approval details

PMA number
P150021
Supplement
S038
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Freestyle Libre Pro Flash Glucose Monitoring System
Generic name
Sensor, glucose, invasive
Applicant
Abbott Diabetes Care, Inc.
Date received
2018-12-26
Decision date
2019-03-19
Days to decision
83 days
Decision code
APPR
Product code
MDS
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Alameda, CA
Statement
Approval for design changes to improve drop, vibration, and shock resistance to the Freestyle Libre Pro Reader.

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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
FreeStyle Libre 3 Continuous Glucose Monitoring System; FreeStyle Libre 2 Flash Glucose Monitoring System (K223435)Abbott Diabetes Care, Inc.2023-04-13
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