Business · 20/02/2014
FDA Withdraws Proposed Rule for Premarket Approval of Shortwave Diathermy Devices
The Food and Drug Administration (FDA) is withdrawing a proposed rule requiring premarket approval for shortwave diathermy devices for all uses, following a review of the Food and Drug Administration Safety and Innovation Act (FDASIA) and new information from a panel meeting.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →