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# Info Collection on Device Q-Submission Program
- URL: https://www.fdaweb.com/info-collection-on-device-q-submission-program/
- Published: 2019-11-15T12:00:00.000Z
- Updated: 2026-09-14T15:53:20.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5145515

*Federal Register* notice: FDA has submitted to OMB an information collection extension for “Q-Submission Program for Medical Devices” (OMB Control Number 0910-0756). The collection concerns a guidance entitled “[Requests for Feedback and Meetings for Medical Device Submissions: The Q-Submission Program](https://www.fda.gov/media/%20114034/download?ref=fdaweb.com)” and provides an overview of the mechanisms available to submitters to request feedback from or a meeting with FDA regarding certain potential or planned medical device submissions. It also provides recommendations regarding certain types of Q-submissions, such as pre-submissions, submission issue requests, study risk determinations, informational meetings, and other Q-submissions types and other uses of the Q-submission program. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2019-11-15/pdf/2019-24803.pdf?ref=fdaweb.com).