FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Automated Insulin Dosing , Threshold Suspend
PMA: P120010
·
Supplement: S061
·
Decision Feb 22, 2016
Classifications
1
FEI Numbers
18
Registration Numbers
18
Basic Information
- Device Name
- Automated Insulin Dosing , Threshold Suspend
- Trade Name
- MiniMed 530G System
- PMA Number
- P120010
- Supplement Number
- S061
- Device Class
- FDA Class 3
- Product Code
- OZO
- Generic Name
- Automated insulin dosing , threshold suspend
- Medical Specialty
- Unknown
- Advisory Committee
- Clinical Chemistry
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- February 22, 2016
- Date Received
- February 6, 2015
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for a change to the shelf height specification for the Enlite Sensor base (part number 6015277-001). The Enlite Sensor base is a subcomponent of Enlite Sensor model MMT-7008, which is a component of the MiniMed 530G System.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| OZO | Automated Insulin Dosing , Threshold Suspend | FDA class 3 | Unknown |