Amplifon S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: AMPLAID A724 AND A728, AMPLAID A315 AND A319, AMPLAID A311 SERIES
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Amplifon S.P.A. Neurology ✕
2 devices