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# Info Collection Revision on Device Labeling
- URL: https://www.fdaweb.com/info-collection-revision-on-device-labeling/
- Published: 2021-10-07T12:00:00.000Z
- Updated: 2026-09-14T17:18:17.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5150318

*Federal Register* notice: FDA has submitted to OMB an information collection revision entitled “Medical Device Labeling Regulations” (OMB Control No. 0910-0485). The collection supports medical device labeling requirements governed by section 502 of the Federal Food, Drug, and Cosmetic Act. Device labeling requirements provide for the label or labeling content of a medical device so that it is not misbranded and subject to regulatory action. To view the notice, click [here](https://public-inspection.federalregister.gov/2021-22043.pdf?ref=fdaweb.com).