FDA Approves ZOLL remedē System for MRI Conditional Use
The United States Food and Drug Administration (FDA) has approved the remedē System, marketed by ZOLL Medical Corporation, for conditional use with magnetic resonance imaging (MRI). ZOLL’s remedē System is an implantable transvenous phrenic nerve stimulation therapy for the treatment of adults with moderate to severe central sleep apnea. Full-body MRI approval applies to all…