Business · 08/11/2005
FDA Proposes Special Controls for Tinnitus Masker Devices
The FDA is proposing to amend the classification regulations of tinnitus masker devices to specify a special control for the device, taking action under the Federal Food, Drug, and Cosmetic Act and the Safe Medical Devices Act of 1990, in response to its own initiative.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →