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# Agfa Multipurpose Imaging System Cleared
- URL: https://www.fdaweb.com/agfa-multipurpose-imaging-system-cleared/
- Published: 2019-02-21T12:00:00.000Z
- Updated: 2026-09-15T01:06:30.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5143441

FDA has cleared an Agfa 510(k) for the DR 800 multipurpose imaging system with tomosynthesis. The device is intended to be one solution for radiography, fluoroscopy, multi-slice and advanced clinical applications. “With the DR 800, Agfa moves from 2D single plane imaging to multi-slice image reconstruction. Tomosynthesis is used to synthesize tomographic slices from a single tomographic sweep,” the company says. “The DR 800 includes Agfa's brand-new, tomosynthesis algorithms for iterative reconstruction, which deliver images with less noise and fewer artifacts.”