Business · 12/06/2014Updated: 10/17/2026 · 1 min read
FDA Withdraws Proposed Rule for Cranial Electrotherapy Stimulator Devices
Summary
The US Food and Drug Administration (FDA) has withdrawn its proposed rule requiring premarket approval for cranial electrotherapy stimulator devices, citing a response to feedback from stakeholders.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →