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# FDA Clears Fresenius Aurora Xi Plasma System
- URL: https://www.fdaweb.com/fda-clears-fresenius-aurora-xi-plasma-system/
- Published: 2016-10-07T12:00:00.000Z
- Updated: 2026-09-14T21:38:04.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5137029

FDA has cleared a Fresenius Kabi 510(k) for the Aurora Xi Plasmapheresis System for use in collecting plasma. “The Aurora Xi system features a proprietary filtration-separation method that enables the faster collection of Source Plasma,” the company says. The device also includes an interactive touch screen, data management capabilities, barcode scanning of donor ID, and an alarm notification system and troubleshooting graphics to help operators resolve issues quickly, it says