Federal Register Notice: FDA’s proposed collection of information, “Medical Devices: Recommended Glossary and Educational Outreach to Support Use of Symbols on Labels and in Labeling of In Vitro Diagnostic Devices Intended for Professional Use — Section 502 of the Federal Food, Drug, and Cosmetic Act/Section 351 of the Public Health Service Act” has been submitted to the Office of Management and Budget for review and clearance under the Paperwork Reduction Act of 1995. To view this notice, click here.