FDA Announces Approval of Medical Devices Collection for Professional Use

Summary

The Food and Drug Administration (FDA) has announced that it has received approval from the Office of Management and Budget (OMB) for a collection of information related to medical devices, including a recommended glossary and educational outreach to support the use of symbols on labels and in labeling of in vitro diagnostic devices intended for professional use, as mandated by the Paperwork Reduction Act of 1995.