FDA 510(k) Applications Submitted by SIEMENS HEARING INSTRUMENTS, INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K011364	05/04/2001	CUSTOM TCI (TINNITUS CONTROL INSTRUMENT)	SIEMENS HEARING INSTRUMENTS, INC.
K011366	05/04/2001	CUSTOM TCI-COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)	SIEMENS HEARING INSTRUMENTS, INC.
K003558	11/17/2000	TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)	SIEMENS HEARING INSTRUMENTS, INC.
K003559	11/17/2000	TCI (TINNITUS CONTROL INSTRUMENT)	SIEMENS HEARING INSTRUMENTS, INC.
K962170	06/05/1996	SIEMENS VITA 160 SERIES POCKET HEARING INSTRUMENT: VITA 162E,166M,168PP	SIEMENS HEARING INSTRUMENTS, INC.
K071462	05/25/2007	UNITY 2 HIA & PROBE ( FOR USE WITH UNITY 2)	SIEMENS HEARING INSTRUMENTS, INC.
K972998	08/12/1997	PRISMA	SIEMENS HEARING INSTRUMENTS, INC.