Amplivox, Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Amplivox, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Deer Field, US.
Historical record: 3 cleared submissions from 2008 to 2017. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Amplivox, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Amplivox, Ltd.
3 devices