Oklahoma HB1915 mandates AI device deployment in healthcare settings comply with FDA regulations and state standards.
Oklahoma HB1915 requires all artificial intelligence devices used in healthcare to adhere to FDA regulations and state standards. Deployers must establish a Quality Assurance Program, maintain an updated inventory of devices, and ensure compliance with federal and state regulations. Qualified end-users, defined as licensed physicians with specific AI training, must review and validate AI-generated data before patient care decisions. Deployers must also monitor device performance, participate in AI assessment registries, and document any overrides or disagreements with AI outputs.
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- Core Provisions
- Implementation
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- Legal Framework
- Critical Issues
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