Atlas FDA

Freestyle Libre Pro Flash Glucose Monitoring System

FDA premarket approval P150021/S042 · decided 2019-06-20

Approval details

PMA number
P150021
Supplement
S042
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Freestyle Libre Pro Flash Glucose Monitoring System
Generic name
Sensor, glucose, invasive
Applicant
Abbott Diabetes Care, Inc.
Date received
2019-05-30
Decision date
2019-06-20
Days to decision
21 days
Decision code
OK30
Product code
MDS
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Alameda, CA
Statement
Manufacturing change in the order of inspections of parts by a vision system during the sensor pack assembly for the Libre sensor. The Libre sensor is a component of the Freestyle Libre Pro Flash Glucose Monitoring System and the Freestyle Libre 14 day Flash Glucose Monitoring System.

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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