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U.S. Department of Health and Human Services

Product Classification

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Device glucose range monitoring system
Definition A glucose range monitoring system (GRM) is intended to automatically measure glucose in the body and provide qualitative or semi-quantitative information about glucose levels or trends continuously or frequently. GRM systems are intended to support general user awareness of glucose ranges related to glycemic control. Outputs from GRM systems do not represent quantitative glucose concentration values and GRM systems are not intended to be used for acute medical decision-making, such as insulin dosing or medication adjustment.
Physical State Glucose sensor, including a mechanism for recording and/or displaying measured glucose ranges. The device contains software to calculate glucose ranges.
Technical Method Sensors that measure glucose levels in the subcutaneous tissue.
Target Area subcutaneous tissue.
Regulation Medical Specialty Clinical Chemistry
Review Panel Clinical Chemistry
Product CodeSFU
Premarket Review Division of Chemistry and Toxicology Devices (DCTD)
Division of Chemistry and Toxicology Devices (DCTD)
Submission Type 510(k)
Regulation Number 862.1359
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting
Ineligible
Implanted Device? No
Life-Sustain/Support Device? No
Third Party Review Not Third Party Eligible
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