US Medical Innovations Secures FDA Clearance for Canady Helios Cold Plasma™ Ablation System
US Medical Innovations, LLC (USMI) announced today it has received FDA 510k Clearance (K240297) for the Canady Helios Cold Plasma™ (CHCP) Ablation System for the ablation of soft tissue during surgery.
- US Medical Innovations, LLC (USMI) announced today it has received FDA 510k Clearance (K240297) for the Canady Helios Cold Plasma™ (CHCP) Ablation System for the ablation of soft tissue during surgery.
- The CHCP system consists of the Canady Helios Cold Plasma XL-1000 CP Smart Electrosurgical Generator, Canady Helios Cold Plasma Ablators, Foot Pedal and Trolley Cart.
- The Canady Helios Cold Plasma™ System introduces a novel approach to soft tissue ablation using plasma.
- For more information on US Medical Innovation’s products and technology please visit: www.usmedinnovations.com .