Business · 13/01/2004Updated: 10/17/2026 · 1 min read
FDA Announces Approval of Medical Device Surveillance Collection
Summary
The Food and Drug Administration (FDA) has received approval from the Office of Management and Budget (OMB) to collect information on postmarket surveillance of medical devices under the Paperwork Reduction Act of 1995.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →