Tinnitus Otosound Products, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tinnitus Otosound Products, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Tinnitus Otosound Products, LLC has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Tinnitus Otosound Products, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tinnitus Otosound Products, LLC
1 devices