Amplifon S.P.A.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K992370AMPLAID A724 AND A728September 20, 1999
K983915AMPLAID A315 AND A319January 29, 1999
K983712AMPLAID A311 SERIESJanuary 12, 1999
K971740AMPLAID MK12March 16, 1998
K974235AMPLAID AM50February 10, 1998
K972959AMPLAID MK22February 6, 1998
K972862AMPLAID 171SOctober 31, 1997
K971747AMPLAID 460August 5, 1997