Business · 27/01/2010Updated: 10/17/2026 · 1 min read
FDA to Enhance 510(k) Review Process for Medical Devices, Host Public Meeting and Solicit Comments
Summary
The US Food and Drug Administration (FDA) is set to strengthen its 510(k) review process for medical devices, with a public meeting scheduled to discuss the changes and a request for comments from the public and industry stakeholders
Original source language: Federal Register — Health and Human ServicesOpen original release →