FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Automated Insulin Dosing , Threshold Suspend
PMA: P120010
·
Supplement: S102
·
Decision Apr 27, 2017
Classifications
1
FEI Numbers
18
Registration Numbers
18
Basic Information
- Device Name
- Automated Insulin Dosing , Threshold Suspend
- Trade Name
- Artificial Pancreas Device System Threshold Suspend
- PMA Number
- P120010
- Supplement Number
- S102
- Device Class
- FDA Class 3
- Product Code
- OZO
- Generic Name
- Automated insulin dosing , threshold suspend
- Medical Specialty
- Unknown
- Advisory Committee
- Clinical Chemistry
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- April 27, 2017
- Date Received
- March 31, 2017
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Additional inspections and inspection equipment by contract manufacturer of introducer needle in the Enlite Sensor and Guardian Sensor (3). The Enlite Sensor is a component of the MiniMed 530G System, the MiniMed 630G System With SmartGuard, the Paradigm Real-Time Revel System with Enlite Sensor, and iPro2 CGM System with Enlite Sensor. The Guardian Sensor (3) is a component of the MiniMed 670G 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 |