sábado, 7 de octubre de 2017

Press Announcements > FDA approves implantable device to treat moderate to severe central sleep apnea

Press Announcements > FDA approves implantable device to treat moderate to severe central sleep apnea





The U.S. Food and Drug Administration today approved a new treatment option for patients who have been diagnosed with moderate to severe central sleep apnea. The Remedē System is an implantable device that stimulates a nerve located in the chest that is responsible for sending signals to the diaphragm to stimulate breathing. Continue reading.

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