for the aura™ CPAP

Minneapolis, MN – April 6, 2005 - AEIOMed™ is pleased to announce that it has received FDA 510(k) clearance for its CPAP, the aura™. It’s the first CPAP system designed from its inception to be truly integrated, with options for a rechargeable battery and heated humidifier. The aura is the newest generation of CPAP technology, offering a compact portable system which eliminates patient compliance excuses based on inconvenience. The aura CPAP brings simplicity and convenience to CPAP users and providers featuring up to 20 cm/H20, automatic altitude compensation, selectable compliance periods and two year warranty.
“All of us at AEIOMed are pleased to receive 510(k) clearance,” said AEIOMed president and CEO Steve Bordewick. “We’ve put our heart and soul into creating the aura CPAP system, we are confident in the difference it will make in the lives of CPAP patients. Now they’ll be able to experience the difference for themselves.”
Apart from its small size including the integrated humidifier and battery options, making it easy to position on a nightstand or slip into a carryon bag, the aura removes the excuses so patients can easily use their CPAP anytime or anywhere. Patients will no longer be constrained by no available power outlet or a bulky separate heated humidifier. The rechargeable battery allows the CPAP unit to charge while the unit is plugged into regular household current or while connected to an optional 12 volt vehicle adapter. The integrated heated humidifier is compact with a well-insulated heating element which prevents accidental contact.
AEIOMed is a privately held, Minneapolis, Minnesota-based medical device company founded on the concept of using better thinking to design and manufacture patented technology for the treatment of sleeps disordered breathing. The aura system, including the aura nasal interface with Headrest™, offers comfort, convenience and portability – removing the excuses for non-compliance.
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