Atlas FDA

Freestyle Libre Pro

FDA premarket approval P160030/S027 · decided 2018-12-21

Approval details

PMA number
P160030
Supplement
S027
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Freestyle Libre Pro
Generic name
Sensor, glucose, invasive, non-adjunctive, factory-calibrated, user-initiated
Applicant
Abbott Diabetes Care, Inc.
Date received
2018-09-27
Decision date
2018-12-21
Days to decision
85 days
Decision code
APPR
Product code
PZE
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Alameda, CA
Statement
Approval for modification of the membrane layer formulation of the FreeStyle Libre and FreeStyle Libre Pro sensor components and an addition of a shipping method for shipment of sensor 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
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