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# Comments Sought on De Novo Device Submissions
- URL: https://www.fdaweb.com/comments-sought-on-de-novo-device-submissions/
- Published: 2017-08-02T12:00:00.000Z
- Updated: 2026-09-14T22:38:13.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5139284

*Federal Register* notice: FDA is seeking comments on a new information collection for “De Novo Classification Process (Evaluation of Automatic Class 3 Designation).” The proposed collection is necessary to satisfy statutory requirements for implementing this voluntary submission program. This follow-up collection includes an estimated hour burden for requests for withdrawal or estimated operating and maintenance costs for eCopy, printing, and shipping of De Novo submissions. To view the notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2017-08-02/pdf/2017-16230.pdf?ref=fdaweb.com).