Amplivox, Ltd. is one of 15052 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Amplivox, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Otowave 302 Portable Tympanometer, Otowave 202 Portable Tympanometer, AMPLIVOX OTOWAVE 102 HAND HELD PORTABLE TYMPANOMETER
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.
Regulatory submissions have been managed by Kamm & Associates and Intertek Testing Services.
FDA 510(k) Regulatory Record - Amplivox, Ltd.
3 devices