Business · 23/12/1997Updated: 10/17/2026 · 1 min read
FDA to Review and Revise Medical Device Compliance Policy Guides and Regulatory Requirements
The FDA is seeking public input on its review of compliance policy guides and regulatory requirements for remarketing used medical devices, with the goal of ensuring these devices meet performance and safety standards.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →