# PZE · Sensor, Glucose, Invasive, Non-Adjunctive, Factory-Calibrated, User-Initiated

_ ·  · Class 3_

**Canonical URL:** https://fda.innolitics.com/productcode/PZE

## Overview

- **Product Code:** PZE
- **Device Name:** Sensor, Glucose, Invasive, Non-Adjunctive, Factory-Calibrated, User-Initiated
- **Regulation:** 21 CFR N/A
- **Device Class:** 3
- **Review Panel:** [](/submissions/)

## Identification

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.

## Recent Cleared Devices (1 of 1)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [P160030](/device/P160030.md) | Freestyle Libre Flash Glucose Monitoring System | Abbott Diabetes Care, Inc. | Sep 27, 2017 | APPR |

## Top Applicants

- Abbott Diabetes Care, Inc. — 1 clearance

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**Source:** [https://fda.innolitics.com/productcode/PZE](https://fda.innolitics.com/productcode/PZE)

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