For Immediate Release: Sept. 16, 2016
Media Inquiries: Theresa Eisenman, 301-796-2969, email@example.com
Consumer Inquiries: 888-INFO-FDA
FDA permits marketing of balloon device to treat persistent Eustachian tube dysfunction
The U.S. Food and Drug Administration today permitted marketing of a device that uses a small balloon to treat persistent Eustachian tube dysfunction (ETD), a condition in which pressure, pain or clogged or muffled sensations occur in the ear.