Atlas FDA

FreeStyle Libre Pro Flash Glucose Monitoring System

FDA premarket approval P150021/S059 · decided 2023-11-21

Approval details

PMA number
P150021
Supplement
S059
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
2023-10-26
Decision date
2023-11-21
Days to decision
26 days
Decision code
OK30
Product code
MDS
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Alameda, CA
Statement
the addition of a verification check to the quality control process used for internally releasing parts for manufacturing of the FreeStyle Libre Pro Flash and FreeStyle Libre 14 day Flash Glucose Monitoring Systems

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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