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# FDA Clears Stereotaxis MAGiC Sweep Catheter
- URL: https://www.fdaweb.com/fda-clears-stereotaxis-magic-sweep-catheter/
- Published: 2025-07-28T12:00:00.000Z
- Updated: 2026-09-14T15:17:35.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5159582

FDA has cleared a Stereotaxis 510(k) for its MAGiC Sweep catheter, which it describes as the world’s first robotically navigated high-density electrophysiology (EP) mapping catheter for diagnosing and treating complex arrhythmia patients. “High density mapping has transformed the EP field, enhancing cardiac ablation procedures by enabling more efficient, detailed and precise identification of arrhythmia origin,” the company says.

Combining high-density mapping with robotics is designed to offer multiple improvements, such as electroanatomical mapping of the heart chambers and precise navigation of the catheter to otherwise difficult to reach areas of the heart, Stereotaxis says. The device’s design improves patient safety with its atraumatic shaft, it adds.