The hospital association urges the FDA to adopt risk-based post-market oversight for AI-enabled medical devices while aligning new requirements with existing regulatory frameworks.
The system integrates updated imaging hardware, AI-driven tools, and independently validated ergonomic features aimed at supporting diagnostic accuracy and user comfort.
As AI becomes embedded in medical equipment, HTM professionals must navigate new questions of accuracy, accountability, and risk.
The hospital association urges the FDA to adopt risk-based post-market oversight for AI-enabled medical devices while aligning new requirements with existing regulatory frameworks.
While adoption is in early stages, executives view artificial intelligence as a way to reduce claim denials, speed up cash flow, and ease administrative burdens.
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The subsidiary will partner with startups and industry to accelerate new imaging technologies, including AI.
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The funding will support the development of an AI platform designed to clean and move large imaging datasets more efficiently than traditional methods.
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The FDA-cleared system uses artificial intelligence to create interactive 3D models from standard medical scans for preoperative planning and intraoperative guidance.
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The agency is requesting public comment on methods for monitoring and evaluating AI models after deployment to ensure continued safety and effectiveness.
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The platform automates calls, messages, and web chats for tasks like appointment booking, reminders, payments, and triage, reducing hold times and freeing up staff time.
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The designation will expedite the review process for the CT-based artificial intelligence, which flags numerous acute conditions simultaneously.
