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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.
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