# Compliance with Section 301 of the Medical Device User Fee and Modernization Act of 2002, as amended – Prominent and Conspicuous Mark of Manufacturers on Single-Use Devices:  Guidance for Industry and FDA Staff - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/compliance-with-section-301-of-the-medical-device-user-fee-and-modernization-act-of-2002-as-amended-prominent-and-conspicuous-mark-of-manufacturers-on-single-use-devices-guidance-for-industry-and-fda-staff/90696dfc-0825-4c69-a6cb-c8ad0d418e1c

> FDA guidance document: Compliance with Section 301 of the Medical Device User Fee and Modernization Act of 2002, as amended – Prominent and Conspicuous Mark of Manufacturers on Single-Use Devices:  Guidance for Industry and FDA Staff. Issue date: May 01, 2006. Get complete insights and analysis.

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## Details

- Title: Compliance with Section 301 of the Medical Device User Fee and Modernization Act of 2002, as amended – Prominent and Conspicuous Mark of Manufacturers on Single-Use Devices:  Guidance for Industry and FDA Staff
- Communication Type: Guidance Document
- Product Type: devices
- Office Name: Center for Devices and Radiological Health
- Office URL: /offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
- Issue Date: 2006-05-01
- Last Changed: 2020-02-28
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2005-D-0156">FDA-2005-D-0156</a>

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