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Articles tagged with “clinical-ai-regulatory-pathway

FDA Clears First LLM as a Medical Device: Inside UpDoc's 510(k)
FDA Clears First LLM as a Medical Device: Inside UpDoc's 510(k)

Analysis of FDA's December 2025 clearance of UpDoc K253281, the first SaMD using patient-facing LLMs in 2026, covering its 510(k) predicate strategy, PCCP, and data on 1,451 AI device clearances.

35 min read
7/4/2026

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