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U.S. Department of Health and Human Services

Product Classification

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Device insulin pump secondary display
Definition The purpose of the insulin pump secondary display is to notify another person of the patient's insulin pump usage information in real time.The secondary display is intended for providing secondary notification of insulin pump usage and does not replace primary real time insulin pump monitoring or standard home blood glucose monitoring.
Physical State Typically a software device installed on a third-party mobile device, or implemented in a web-based platform.
Technical Method Receives and displays real-time patient data from an insulin pump.
Target Area n/a
Regulation Medical Specialty Clinical Chemistry
Review Panel Clinical Chemistry
Product CodePKU
Premarket Review Office of In Vitro Diagnostics and Radiological Health (OIR)
Submission Type 510(K) Exempt
Regulation Number 862.1350
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
    Note: Class II devices the Food and Drug Administration (FDA) has also published a list of Class II (special controls) devices subject to certain limitations, that are now exempt from the premarket notification requirements under the Food and Drug Administration Modernization Act of 1997 (the Modernization Act). FDA believes that these exemptions will relieve manufacturers from the need to submit premarket notification submissions for these devices and will enable FDA to redirect the resources that would be spent on reviewing such submissions to more significant public health issues. FDA is taking this action in order to meet a requirement of the Modernization Act.
Implanted Device? No
Life-Sustain/Support Device? No
Third Party Review Not Third Party Eligible