SeeMedX Files 510(k) with FDA for Innovative Cardiac Monitoring System to Transform Heart Failure Care

LAS VEGAS, Nov. 4, 2024 /PRNewswire/ -- SeeMedX Inc. ("SeeMedX") today announced the submission of its 510(k) premarket notification to the U.S. Food and Drug Administration (FDA) for its innovative, non-invasive cardiac monitoring device, designed to allow medical professionals to have real-time insights into cardiac performance and fluid status

“This submission marks a major milestone for SeeMedX in advancing heart failure care,” said Deborah Simpson, CEO of SeeMedX. “After the unexpected loss of my father, I made it my personal mission to develop a life-changing solution for heart failure treatment. Our goal is to empower clinicians with tools that ultimately improve outcomes for patients everywhere.” 

Healthcare professionals often face limited choices dominated by invasive, high-risk, and costly options.

Why SeeMedX is Transformative for Heart Failure Treatment
SeeMedX’s non-invasive cardiac device provides precise hemodynamic measurements including Zo (fluid status) and CO (cardiac output), allowing clinicians to detect volume overload and other heart failure symptoms earlier than traditional methods.

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