# 2025-13050: FDA Seeks Thoughts on Device Dev Tools and Feedback Programs

2025-13050, Agency Information Collection Activities; Proposed Collection; Comment Request; Q-Submission and Early Payor Feedback Request Programs and Medical Device Development Tools, is a Federal Register notice from Health and Human Services Department, Food and Drug Administration published 2025-07-14, effective 60 days for public comment in response to the notice. (as of 2026-06-08).

- Canonical: https://policyrisk.com/federal-register/2025-13050
- As of: 2026-06-08
- Plain-text twin of the page above; the HTML and this file carry the same facts.

## Facts
- Document number: 2025-13050
- Title: Agency Information Collection Activities; Proposed Collection; Comment Request; Q-Submission and Early Payor Feedback Request Programs and Medical Device Development Tools
- Type: Notice
- Agencies: Health and Human Services Department; Food and Drug Administration
- Citation: 90 FR 31225
- Published: 2025-07-14
- Effective: 60 days for public comment in response to the notice.
- Comments close: not stated
- Significant: no
- Touches household money: no
- Regulation identifier numbers: none
- Last updated: 2026-06-08

## In one line

FDA Seeks Thoughts on Device Dev Tools and Feedback Programs

## Summary

The FDA wants your thoughts on how they collect info about medical device feedback programs and tool qualifications. If you’re involved in making or paying for medical devices, this could affect you. They’re asking for comments over the next 60 days to help improve the process—no extra costs, just your input!

## Abstract

The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed revision of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on information collection requirements associated with the Q-Submission and Early Payor Feedback Request Programs for medical devices and Qualification of Medical Device Development Tools.

## Effects PRIA read

No economic effects identified for this document.

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## Sources
- [2025-13050 on federalregister.gov](https://www.federalregister.gov/documents/2025/07/14/2025-13050/agency-information-collection-activities-proposed-collection-comment-request-q-submission-and-early)
- [2025-13050 as published (PDF)](https://www.govinfo.gov/content/pkg/FR-2025-07-14/pdf/2025-13050.pdf)

## Related
- [Previous: 2025-13049, Agency Information Collection Activities; Proposed Collection; Comment Request;…](https://policyrisk.com/federal-register/2025-13049)
- [Next: 2025-13051, National Institute of Environmental Health Sciences; Notice of Meeting](https://policyrisk.com/federal-register/2025-13051)
- [All Federal Register documents](https://policyrisk.com/federal-register)

Source: PRIA, https://policyrisk.com/federal-register/2025-13050 (as of 2026-06-08).