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Business · 22/02/2024Updated: 10/17/2026 · 1 min read

FDA Announces Availability of Draft Guidance for Small Business Medical Device User Fee Waiver

Summary

The Food and Drug Administration (FDA) has released a draft guidance outlining how it will determine if a small business is experiencing financial hardship and eligible for a waiver of their medical device registration fee, with the guidance set to be finalized at a later date.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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