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# FDA Clears HemoSphere Hemodynamics Monitor
- URL: https://www.fdaweb.com/fda-clears-hemosphere-hemodynamics-monitor/
- Published: 2017-04-19T12:00:00.000Z
- Updated: 2026-09-14T22:18:25.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5138491

FDA has cleared an Edwards Lifesciences 510(k) for its HemoSphere advanced monitoring platform that is intended to provide clinicians with information on a patient’s hemodynamics. The device allows clinicians to “choose the clinical support screens that best suit their needs and monitor the pressures and blood flow of the right heart as conditions change, informing potentially life-saving decisions on behalf of their patients,” the company says. It is also compatible with Edwards Swan-Ganz pulmonary artery catheter and Oximetry catheters.