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ENLITE SENSOR

FDA premarket approval P120010/S001 · decided 2015-10-02

Approval details

PMA number
P120010
Supplement
S001
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ENLITE SENSOR
Generic name
Automated insulin dosing , threshold suspend
Applicant
Medtronic, Inc.
Date received
2013-11-06
Decision date
2015-10-02
Days to decision
695 days
Decision code
APPR
Product code
OZO
Advisory committee
Clinical Chemistry
Expedited review
No
Location
Northridge, CA
Statement
APPROVAL FOR ADDING DUPLICATE EXISTING MANUFACTURING STEPS TO THE PREPARATION OF BULK GLUCOSE OXIDASE (GOX) PERFORMED BY THE SUPPLIER FOR USE IN THE SPONSOR¿S ENLITE SENSOR (MODEL: MMT-7008) AND SOF-SENSOR (MODELS: MMT-7002 AND MMT-7003) DEVICES. THE ENLITE SENSOR IS A COMPONENT OF THE MINIMED 530G SYSTEM. THE SOF-SENSOR IS A COMPONENT OF THE PARADIGM REAL-TIME, PARADIGM REALTIME REVEL, GUARDIAN REAL-TIME, MINILINK REAL-TIME, IPRO RECORDER AND IPRO2 PROFESSIONAL CONTINUOUS GLUCOSE MONITORING SYS

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