Atlas FDA

Freestyle Libre Pro Flash Glucose Monitoring System

FDA premarket approval P160030/S038 · decided 2019-09-12

Approval details

PMA number
P160030
Supplement
S038
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, non-adjunctive, factory-calibrated, user-initiated
Applicant
Abbott Diabetes Care, Inc.
Date received
2019-08-15
Decision date
2019-09-12
Days to decision
28 days
Decision code
OK30
Product code
PZE
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Alameda, CA
Statement
Update to the shipping pallet configuration, removal of the temperature controls from shipping, and extending in-process shelf life of foil-bagged glucose sensor reels. The glucose sensor is a component of the FreeStyle Libre 14-day and FreeStyle Libre Pro 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