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Samples in periodicals archive:
a leading developer of innovative respiratory assist devices, announced today that it has received CE Mark approval for its Hemolung Respiratory Assist System (RAS).
Food and Drug Administration has granted the company 510(k) clearance to market its CARDIOHELP System in the United States as a cardiac and/or respiratory assist device for up to six hours.
The OSA and COPD diagnosed patient is initially required to begin their therapy with a respiratory assist device (a device without a backup rate) and can only receive a NPPV device with a backup rate if it can be documented that the respiratory assist device is ineffective.