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# Guides on Device Surveillance/Post-approval Studies
- URL: https://www.fdaweb.com/guides-on-device-surveillance-post-approval-studies/
- Published: 2022-10-10T12:00:00.000Z
- Updated: 2026-09-14T18:02:27.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5152929

*Federal Register* notice: FDA is making available final guidances entitled “Postmarket Surveillance Under Section 522 of the Federal Food, Drug, and Cosmetic Act” and “Procedures for Handling Post-Approval Studies Imposed by PMA \[Premarket Approval Application\] Order.” The documents are intended to increase transparency to stakeholders on FDA’s approach to issuing and tracking postmarket surveillance orders and post-approval study requirements. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2022-10-07/pdf/2022-21832.pdf?ref=fdaweb.com).