Atlas FDA

Freestyle Libre Flash Glucose Monitoring System

FDA premarket approval P160030/S001 · decided 2017-12-08

Approval details

PMA number
P160030
Supplement
S001
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
Freestyle Libre Flash Glucose Monitoring System
Generic name
Sensor, glucose, invasive, non-adjunctive, factory-calibrated, user-initiated
Applicant
Abbott Diabetes Care, Inc.
Date received
2017-10-20
Decision date
2017-12-08
Days to decision
49 days
Decision code
APPR
Product code
PZE
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Alameda, CA
Statement
Approval of the protocol for the post-approval study (PAS) protocol.

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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