FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Sensor, Glucose, Invasive
PMA: P980022
·
Supplement: S090
·
Decision Jan 7, 2011
Classifications
1
FEI Numbers
23
Registration Numbers
23
Basic Information
- Device Name
- Sensor, Glucose, Invasive
- Trade Name
- MEDTRONIC MINIMED CONTINUOUS GLUCOSE MONITORING SYSTEM
- PMA Number
- P980022
- Supplement Number
- S090
- Device Class
- FDA Class 3
- Product Code
- MDS
- Generic Name
- Sensor, glucose, invasive
- Medical Specialty
- Unknown
- Advisory Committee
- Clinical Chemistry
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- January 7, 2011
- Date Received
- November 8, 2010
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A MODIFICATION TO THE DESIGN SPECIFICATION OF THE LUMEN TUBING USED IN THE MANUFACTURING PROCESS OF THE GLUCOSE SENSOR TO ALLOW FOR LESS DIMENSIONAL VARIATION IN THE TUBING SUPPLIED BY THE TUBING VENDOR.
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 |
|---|---|---|---|
| MDS | Sensor, Glucose, Invasive | FDA class 3 | Unknown |