Business · 26/05/2006Updated: 10/17/2026 · 1 min read
FDA Seeks Public Comment on Proposed Collection of Investigational Device Exemptions Reports and Records
Summary
The Food and Drug Administration (FDA) is requesting public input on a proposed collection of information related to Investigational Device Exemptions Reports and Records, as required by the Paperwork Reduction Act of 1995.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →