HB 1915 Summary

• Defines artificial intelligence (AI) medical devices, deployers (hospitals/physician practices), and qualified end-users (licensed physicians with independent diagnostic capability and AI-specific training) for use in Oklahoma health care settings.

• Requires AI devices to be deployed and utilized in accordance with FDA regulations and federal guidance, and mandates exclusive use by qualified end-users.

• Mandates deployers implement a Quality Assurance Program, conduct regular performance evaluations, document AI device-generated data reviews, and maintain records of instances where qualified end-users override or disagree with device outputs.

• Requires deployers to establish an AI governance group with qualified end-user representation, maintain updated device inventories with safety documentation, conduct diligent selection processes, document use cases and training procedures, and continuously monitor device performance with participation in national specialty society registries when feasible.

• Grants the State Department of Health authority to enforce the act and establish penalties for noncompliance; becomes effective November 1, 2025.