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Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Adverse Event Program for Medical Devices: (Medical Product Safety Network (MedSun))
Comment period open: closes in 23 days (Nov 9, 2026). Comment on Regulations.gov →
Read on FederalRegister.gov · Official PDF · Docket on Regulations.gov · Submit a comment · Add to calendar (.ics)
Summary (from the Federal Register abstract)
The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.
- Document type
- Notice
- Federal Register document number
- 2026-20661
- Published
- Oct 8, 2026
- Action
- Notice.
- Docket
- FDA-2026-N-7129
- Comments posted on Regulations.gov (at last check)
- 0
- DATES section (from the document)
- Submit written comments (including recommendations) on the collection of information by November 9, 2026.
- Topics (auto-tagged)
- Medical devices
Source: Federal Register API, document 2026-20661. Federal Register text is a U.S. government work. Confirm dates in the official document; later documents may extend, reopen or correct them.