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
FDA 510(k) Regulatory Record - Amplivox, Ltd. Ear, Nose, Throat ✕
3 devices