← FDA Medical Device Classifications

Sensor, Glucose, Invasive, Non-Adjunctive, Factory-Calibrated, User-Initiated

PZE · Class III — High Risk (PMA approval required, life-sustaining) · Unknown

Classification

FDA Product Code
PZE
Device class
Class III — High Risk (PMA approval required, life-sustaining)
Regulation
Review panel
CH
Medical specialty
Unknown
Submission type
2
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
N

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.

Market data

Cleared 510(k) submissions
0
Registered establishments
11

Source

Authoritative
FDA Device Classification database
Machine
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