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Business · 05/06/2026Updated: 10/17/2026 · 1 min read

FDA Announces Guidance on Exempting Unclassified Medical Devices from Premarket Notification Requirements

Summary

The FDA is releasing a guidance document outlining its plan to exempt certain unclassified medical devices from premarket notification requirements, based on current standards and available information.

Original source language: Federal Register — Health and Human ServicesOpen original release →

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