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# Info Collection on Device Postmarket Surveillance
- URL: https://www.fdaweb.com/info-collection-on-device-postmarket-surveillance/
- Published: 2022-05-26T12:00:00.000Z
- Updated: 2026-09-14T17:46:26.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5151912

*Federal Register* notice: FDA is seeking comments on an information collection extension entitled “Postmarket Surveillance of Medical Devices — 21 CFR Part 822” (OMB Control Number 0910-0449). The collection supports FDA’s authority to require a manufacturer to conduct postmarket surveillance on any device that meets the criteria set forth in the statute. To view the notice, click [here](https://public-inspection.federalregister.gov/2022-11412.pdf?ref=fdaweb.com).