FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Automated Insulin Dosing , Threshold Suspend
PMA: P120010
·
Supplement: S113
·
Decision Mar 7, 2018
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
- S113
- 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
- March 7, 2018
- Date Received
- February 9, 2018
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for a minor design change to the introducer needle component of the Guardian Sensor (3) and the Enlite Sensor and the addition of an alternate needle supplier.
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 |