> ## Content Index
> Fetch the complete content index at: https://www.fdaweb.com/llms.txt
> Use this file to discover other available public pages before exploring further.

# 510(k) Required for Powered Patient Transports: FDA
- URL: https://www.fdaweb.com/510-k-required-for-powered-patient-transports-fda/
- Published: 2021-12-07T12:00:00.000Z
- Updated: 2026-09-14T17:24:50.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5150710

*Federal Register* notice: FDA is publishing an order on its final determination involving a petition requesting exemption from premarket notification (510(k)) requirements for the generic device type: powered patient transport (product code ILK). FDA has determined that premarket notification is necessary to provide a reasonable assurance of the safety and effectiveness of such devices. To view the notice, click [here](https://public-inspection.federalregister.gov/2021-26636.pdf?ref=fdaweb.com).