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# Guide on 510(k) 3rd Party Review Program
- URL: https://www.fdaweb.com/guide-on-510-k-3rd-party-review-program/
- Published: 2020-03-12T12:00:00.000Z
- Updated: 2026-09-14T16:06:57.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5146312

*Federal Register* notice: FDA has made available a final guidance entitled “510(k) Third Party Review Program.” The document provides a comprehensive look into FDA’s current thinking regarding the 510(k) Third Party Review Program. It discusses factors that will be used in determining whether a Class 1 or Class 2 device type, or subset of such device types, is eligible for review by an accredited person. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2020-03-12/pdf/2020-05080.pdf?ref=fdaweb.com).