PZE — Sensor, Glucose, Invasive, Non-Adjunctive, Factory-Calibrated, User-Initiated Class III
FDA product code PZE covers "Sensor, Glucose, Invasive, Non-Adjunctive, Factory-Calibrated, User-Initiated", a Class III medical device. Submissions are reviewed by the Unknown panel.
Classification Details
- Product Code
- PZE
- Device Class
- Class III
- Regulation Number
- Submission Type
- Review Panel
- CH
- Medical Specialty
- Unknown
- Implant
- No
Definition
A subcutaneous factory calibrated, non-adjunctive, invasive, passive monitoring glucose sensor is intended to determine glucose levels and the direction and rate of change of glucose levels in people with diabetes. Calibrated at the point of manufacture and does not require or accept any user-entered calibration. Monitors glucose levels passively and only provides information, including alarms and alerts, in response to a user initiated action. The device is indicated to replace information obtained from standard blood glucose monitoring devices to make diabetes-related treatment decisions and also provides historical glucose information, facilitating long-term therapy adjustments.