Physio-Control announces FDA clearance for new chest compression system

Tue. June 30, 2009; Posted: 09:37 AM

Jun 30, 2009 (Datamonitor via COMTEX) -- MDT | Quote | Chart | News | PowerRating -- Physio-Control, a wholly owned subsidiary of Medtronic, has reported that Lucas 2, the next-generation Lucas chest compression system, has received 510(k) market clearance from the FDA.

Developed and manufactured by Jolife and distributed exclusively in the US by Physio-Control, the Lucas 2 is an automated, battery-powered device that is designed to give consistent, uninterrupted compressions to victims in cardiac arrest, said Medtronic.

By ensuring consistent blood flow, Lucas helps emergency medical responders deliver a more viable candidate for recovery to the emergency department, added Medtronic. Furthermore, Lucas can assist in improving the operations of an emergency response system or hospital by helping to reduce the chaos on the scene and free up staff for other emergencies, noted Medtronic.

Lucas 2 builds upon the Lucas 1 technology, but differs from its predecessor in that it is an electric rather than a pneumatic device. Lucas 2 can be powered either by battery alone or using a wall or car electricity outlet. The battery is the latest in rechargeable, lithium ion polymer technology and operates for up to 45 minutes (typical) on a single battery, the company said.

Lucas 2 is also equipped with Smart Restart functionality. Lucas 2 offers other new features such as alerts and pauses to aid ventilation during compressions with an unsecured airway (bag-valve-mask) and quieter operation, according to Medtronic.

Erik von Schenck, CEO of Jolife, said: "With the Lucas 2 we now offer a solution to customers that prefer a battery-powered device, and the Lucas 1 for those who prefer the pneumatic solution. The rechargeable battery requires a minimum of maintenance, and makes the device the most compact, lightweight and portable mechanical chest compression device on the market."

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