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# Device User Fee Rates for FY 2022
- URL: https://www.fdaweb.com/device-user-fee-rates-for-fy-2022/
- Published: 2021-07-30T12:00:00.000Z
- Updated: 2026-09-14T17:08:38.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5149833

*Federal Register* notice: FDA has set the medical device user fee rates for fiscal year 2022\. The standard fees are as follows: PMA or efficacy supplement ($374,858); panel-track supplement ($281,143); de novo classification request ($112,457); 180-day supplement ($56,229); real-time supplement ($26,240); and 510(k) premarket notification submission ($12,745). To view the notice, click [here](https://public-inspection.federalregister.gov/2021-16408.pdf?ref=fdaweb.com).