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# Info Collection on Device Allegations Submitted to CDRH
- URL: https://www.fdaweb.com/info-collection-on-device-allegations-submitted-to-cdrh/
- Published: 2020-09-04T12:00:00.000Z
- Updated: 2026-09-14T16:27:48.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5147589

*Federal Register* notice: FDA has submitted to OMB an information collection extension for “Electronic Submission Process for Voluntary Allegations to the Center for Devices and Radiological Health” (OMB Control Number 0910-0769). The collection supports information voluntarily submitted to CDRH on actual or potential health risk concerns about a medical device or radiological product or its use. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2020-09-04/pdf/2020-19563.pdf?ref=fdaweb.com).