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# 1,003 Class 2 Devices Exempted from 510(k)
- URL: https://www.fdaweb.com/1-003-class-2-devices-exempted-from-510-k/
- Published: 2017-07-11T12:00:00.000Z
- Updated: 2026-09-14T22:33:27.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5139103

*Federal Register* notice: FDA has announced a list of 1,003 Class 2 devices that it has determined no longer require premarket notification to provide reasonable assurance of safety and effectiveness, subject to certain limitations. This notice represents FDA’s final determination on a proposed list of devices published 3/14\. The exemptions in this notice are intended to decrease regulatory burdens on the medical device industry and will eliminate private costs and expenditures required to comply with certain federal regulations. To view the notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2017-07-11/pdf/2017-14453.pdf?ref=fdaweb.com).