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# 510(k) Information Collection Procedures Revised
- URL: https://www.fdaweb.com/510-k-information-collection-procedures-revised/
- Published: 2020-04-16T12:00:00.000Z
- Updated: 2026-09-14T16:11:32.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5146586

*Federal Register* notice: FDA has submitted to OMB an information collection revision entitled “Premarket Notification Procedures — 21 CFR Part 807, Subpart E” (OMB Control Number 0910–0120). The revision addresses electronic submission templates that will serve as guided submission preparation tools for industry to improve submission consistency and enhance efficiency in the review process. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2020-04-16/pdf/2020-08011.pdf?ref=fdaweb.com).