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# Comments Sought on Device Reclassification Info Collection
- URL: https://www.fdaweb.com/comments-sought-on-device-reclassification-info-collection/
- Published: 2018-03-07T12:00:00.000Z
- Updated: 2026-09-14T23:28:23.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5140931

*Federal Register* notice: FDA is seeking comments on an information collection for “Reclassification Petitions for Medical Devices — 21 CFR Section 860.123” (OMB Control Number 0910-0138). Reclassification provisions of the Food, Drug & Cosmetic Act allow any person to petition for reclassification of a device from any of the three classes (Class 1, 2 or 3) to another class. The agency’s reclassification content regulation requires the submission of valid scientific evidence demonstrating that the proposed reclassification will provide a reasonable assurance of safety and effectiveness of the device type for its indications for use. To view the notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2018-03-07/pdf/2018-04613.pdf?ref=fdaweb.com).