FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Automated Insulin Dosing , Threshold Suspend
PMA: P120010
·
Supplement: S012
·
Decision Mar 21, 2014
Classifications
1
FEI Numbers
18
Registration Numbers
18
Basic Information
- Device Name
- Automated Insulin Dosing , Threshold Suspend
- Trade Name
- ENLITE SENSOR
- PMA Number
- P120010
- Supplement Number
- S012
- 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
- March 21, 2014
- Date Received
- February 20, 2014
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
NEW LASER TECHNOLOGY SYSTEM TO CUT A RECTANGULAR WINDOW IN THE SENSOR TUBE FOR THE ENLITE SENSOR (MMT-7008A, MMT-7008B). THE ENLITE SENSOR 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 |