Business · 05/12/2016Updated: 10/17/2026 · 1 min read
FDA Seeks Public Comment on Proposed Medical Device Information Collection for OMB Review
Summary
The Food and Drug Administration (FDA) is requesting public comment on a proposed collection of information for review and clearance under the Paperwork Reduction Act of 1995, which will impact medical device manufacturers.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →