Business · 17/01/2014Updated: 10/17/2026 · 1 min read
FDA Announces Premarket Approval of Medical Devices Under Paperwork Reduction Act
Summary
The Food and Drug Administration (FDA) has announced that it has received approval from the Office of Management and Budget (OMB) to collect information on medical devices under the Paperwork Reduction Act of 1995, as required for Premarket Approval of Medical Devices--21 CFR Part 814.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →