Atlas FDA

iPro2 CGM System with Enlite Sensor

FDA premarket approval P150029/S032 · decided 2019-11-22

Approval details

PMA number
P150029
Supplement
S032
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
iPro2 CGM System with Enlite Sensor
Generic name
Sensor, glucose, invasive
Applicant
Medtronic Minimed
Date received
2019-09-30
Decision date
2019-11-22
Days to decision
53 days
Decision code
OK30
Product code
MDS
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Northridge, CA
Statement
Addition of an automated needle hub assembly line for the construction of the Enlite and the Guardian (3) sensors. The Enlite and Guardian (3) sensors are a component of the Minimed, Paradigm, and Ipro2 systems.

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510(k) clearances by this applicant

RecordFirmDate
SmartGuard Technology; Predictive Low Glucose Technology (K261962)Medtronic MiniMed2026-07-09
SmartGuard Technology; Predictive Low Glucose Technology (K253701)Medtronic Minimed2026-02-03
MiniMed Go App (K253512)Medtronic Minimed2026-01-08
InPen System App (MMT-8060 (iOS), MMT-8061 (Android)) (K242775)Medtronic Minimed2024-11-12
Extended Reservoir; MiniMed Reservoir (K241622)Medtronic Minimed2024-07-02
MiniMed Quick-serter (K160860)Medtronic Minimed2016-09-22
MEDTRONIC MINIMED PARADIGM INSULIN PUMPS (K120206)Medtronic Minimed2012-03-29
POLYFIN INFUSION SET, MODELS MMT-165, MMT-365, MMT-366, MMT-312S AND MMT-312L AND SOF-SET INFUSION SETS (K100432)Medtronic Minimed2010-07-09