FDA 510(k) Applications Submitted by AMPLIFON S.P.A.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K971740	05/12/1997	AMPLAID MK12	AMPLIFON S.P.A.
K971747	05/12/1997	AMPLAID 460	AMPLIFON S.P.A.
K992370	07/15/1999	AMPLAID A724 AND A728	AMPLIFON S.P.A.
K972862	08/04/1997	AMPLAID 171S	AMPLIFON S.P.A.
K972959	08/11/1997	AMPLAID MK22	AMPLIFON S.P.A.
K983712	10/21/1998	AMPLAID A311 SERIES	AMPLIFON S.P.A.
K983915	11/04/1998	AMPLAID A315 AND A319	AMPLIFON S.P.A.
K974235	11/12/1997	AMPLAID AM50	AMPLIFON S.P.A.