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Business · 01/04/2010Updated: 10/17/2026 · 1 min read

FDA Expands Medical Device Regulations to Include Pediatric Subpopulations

Summary

The FDA is amending its regulations on premarket approval of medical devices to require the submission of information on pediatric subpopulations that suffer from the disease or condition a device is intended to treat, diagnose, or cure.

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

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