MINIMED 530G SYSTEM
FDA premarket approval P120010/S088 · decided 2016-04-27
Approval details
- PMA number
- P120010
- Supplement
- S088
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- MINIMED 530G SYSTEM
- Generic name
- Automated insulin dosing , threshold suspend
- Applicant
- Medtronic, Inc.
- Date received
- 2016-03-28
- Decision date
- 2016-04-27
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- OZO
- Advisory committee
- Clinical Chemistry
- Expedited review
- No
- Location
- Northridge, CA
- Statement
- Change to incorporate a step that allows the operators to wipe excess Glucose Oxidase (GOx) material from the plate during Enlite glucose sensor manufacturing. The Enlite glucose sensor is a component of the MiniMed 530G System, and the Paradigm REAL-Time REVEL System with Enlite Sensor.
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