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# Info Collection on Device 513(g) Info Requests
- URL: https://www.fdaweb.com/info-collection-on-device-513-g-info-requests/
- Published: 2021-01-12T12:00:00.000Z
- Updated: 2026-09-14T16:42:21.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5148422

*Federal Register* notice: FDA is seeking comments on an information collection extension entitled “513(g) Request for Information” (OMB Control Number 0910-0705). The collection supports an agency guidance on *FDA and Industry Procedures for Section 513(g) Requests for Information Under the Federal Food, Drug, and Cosmetic Act*, which establishes procedures for submitting, reviewing, and responding to requests for information respecting the class in which a device has been classified or the requirements applicable to a device under the FD&C Act that are submitted in accordance with section 513(g). To view the notice, click [here](https://public-inspection.federalregister.gov/2021-00470.pdf?ref=fdaweb.com).