Etymotic Research, Inc. is one of 15057 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Etymotic Research, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ER36 Series OAE Test System, ER35 ERO-SCAN PRO HEARING TEST SYSTEM, ER35 ERO-SCAN PRO HEARING TEST SYSTEM
3
Total
3
Cleared
0
Denied
Etymotic Research, Inc. has 3 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 3 cleared submissions from 2007 to 2015. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Etymotic Research, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Nsf Health Sciences Medical Devices as regulatory consultant.
FDA 510(k) Regulatory Record - Etymotic Research, Inc.
3 devices