Federal Register Notice: FDA has submitted a proposed collection of information, “Premarket Approval of Medical Devices — 21 CFR Part 814 and Food and Drug Administration Modernization Act Sections 201, 202, 205, 208, and 209” to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. To view this notice, click here.
