# 510(k) Third Party Review Program and Third Party Emergency Use Authorization (EUA) Review:  Guidance for Industry, Food and Drug Administration Staff, and Third Party Review Organizations - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/510k-third-party-review-program-and-third-party-emergency-use-authorization-eua-review-guidance-for-industry-food-and-drug-administration-staff-and-third-party-review-organizations/1bdc19b2-0e5f-47a4-aa74-15e3e730ff5c

> FDA guidance document: 510(k) Third Party Review Program and Third Party Emergency Use Authorization (EUA) Review:  Guidance for Industry, Food and Drug Administration Staff, and Third Party Review Organizations. Issue date: November 21, 2024. Get complete insights and analysis.

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## Details

- Title: 510(k) Third Party Review Program and Third Party Emergency Use Authorization (EUA) Review:  Guidance for Industry, Food and Drug Administration Staff, and Third Party Review Organizations
- 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: 2024-11-21
- Last Changed: 2024-11-20
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2016-D-2565">FDA-2016-D-2565</a>

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