Medical Device User Fee Small Business Qualification and Certification; Guidance for Industry, Food and Drug Administration Staff, and Foreign Governments | Federal Regulations · Congress.wiki

Nonrulemaking

FDA

Open for Comments

FDA-2018-D-1873

Medical Device User Fee Small Business Qualification and Certification; Guidance for Industry, Food and Drug Administration Staff, and Foreign Governments

Documents

Comments

Description

OPEN

Key Dates

Comment Period OpensJan 17, 2024

Comment Period ClosesJul 10, 2025

Documents

Type	Title	Posted	Comments	Status
Notice	Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals FR Doc: 2025-18621	Sep 25, 2025	--

Comment Statistics

Total Comments

Keywords

CDER

Medical Device User Fee Small Business

Qualification and Certification

Guidance for Industry

OPEN

Data from Regulations.gov