FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Automated Insulin Dosing , Threshold Suspend
PMA: P120010
·
Supplement: S058
·
Decision Jun 9, 2015
Classifications
1
FEI Numbers
18
Registration Numbers
18
Basic Information
- Device Name
- Automated Insulin Dosing , Threshold Suspend
- Trade Name
- ENLITE GLUCOSE SENSOR
- PMA Number
- P120010
- Supplement Number
- S058
- 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
- June 9, 2015
- Date Received
- January 26, 2015
- Supplement Type
- 135 Review Track For 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A CHANGE IN THE PRE-DOSING PROCESS OF THE ENLITE SENSORADHESIVE PATCH. THE ENLITE SENSOR (MMT-7008) 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 |