3 results
Approved WMOCompleted
To obtain the safety and effectiveness data necessary to support a Premarket Approval (PMA) Application to the U.S. Food and Drug Administration (FDA)
Approved WMOCompleted
To determine the efficacy and safety of the CardioFit system for the treatment of subjects with systolic heart failure who have failed to achieve symptom relief through standard evidence-based management per applicable guidelines.
Approved WMOCompleted
Through this research, we want to further investigate the concept of ear molding through the use of the EarWell Infant Corrective System, this time in the Dutch population. We hope to investigate the opinion on the treatment within the Dutch…