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# Comments Sought on Info Collection Under 513(g) Devices
- URL: https://www.fdaweb.com/comments-sought-on-info-collection-under-513-g-devices/
- Published: 2017-11-21T12:00:00.000Z
- Updated: 2026-09-14T23:02:59.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5140177

*Federal Register* notice: FDA is seeking comments on an information collection extension for “513(g) Request for Information OMB Control Number 0910-0705.” Section 513(g) of the Federal Food, Drug, and Cosmetic Act discusses how sponsors obtain the agency’s views about the classification and regulatory requirements that may be applicable to a particular device. An associated guidance exists, “FDA and Industry Procedures for Section 513(g) Requests for Information Under the Federal Food, Drug, and Cosmetic Act; Guidance for Industry and Food and Drug Administration Staff” that outlines procedures for submitting, reviewing, and responding such requests. To view the notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2017-11-21/pdf/2017-25159.pdf?ref=fdaweb.com).