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# Device Postmarket Surveillance Info Collection
- URL: https://www.fdaweb.com/device-postmarket-surveillance-info-collection/
- Published: 2022-11-07T12:00:00.000Z
- Updated: 2026-09-14T18:05:23.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5153138

*Federal Register* notice: FDA has submitted to OMB an information collection extension entitled “Postmarket Surveillance of Medical Devices — 21 CFR Part 822” (OMB Control Number 0910-0449). Agency regulations establish procedures that it uses to approve and disapprove postmarket surveillance plans. The regulation provides instructions to manufacturers, so they know what information is required in a plan’s submission. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2022-11-07/pdf/2022-24232.pdf?ref=fdaweb.com).