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# Comments Sought on eSubmissions for CDRH Product Complaints
- URL: https://www.fdaweb.com/comments-sought-on-esubmissions-for-cdrh-product-complaints/
- Published: 2017-08-24T12:00:00.000Z
- Updated: 2026-09-14T22:43:15.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5139469

*Federal Register* notice: FDA is seeking comments on an information collection entitled “Electronic Submission Process for Voluntary Allegations to the Center for Devices and Radiological Health — OMB Control Number 0910–0769.” The collection requests information voluntarily submitted to CDRH on actual or potential health risk concerns about a medical device or radiological product or its use. The information provided in the allegations received by CDRH may be used to clarify the recurrence or emergence of significant device-related risks to the general public and the need to initiate educational outreach or regulatory action to minimize or mitigate identified risks. To view the notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2017-08-23/pdf/2017-17836.pdf?ref=fdaweb.com).