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# FDA Clears GE Pulse Imaging System
- URL: https://www.fdaweb.com/fda-clears-ge-pulse-imaging-system/
- Published: 2023-10-18T12:00:00.000Z
- Updated: 2026-09-14T14:13:36.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5155599

FDA has cleared a GE HealthCare 510(k) for its Allia IGS Pulse imaging system. The device features a monopolar x-ray tube used to capture images for interventional procedures. “The small footprint of the new tube also helps clinicians reach steep angulation for better understanding of coronary artery anatomy, even with the 30cm detector configurations,” the company says. The device is also designed to obtain “exceptional image quality for large and bariatric patients with a BMI of greater than 30,” it says. Additionally, its reduced pulse width and X-ray peak power helps to decrease “motion blur” for better visualization of moving elements such as vessels and devices, according to GE.