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Gn Danavox, Inc.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K971031	AUDALLION III HEARING SYSTEM	ESD	1997-06-17	View
510(k)	K971032	DANAVOX MODELS 163/162 BTE	ESD	1997-06-17	View
510(k)	K942331	DANAVOX MODEL CIC	ESD	1994-11-15	View
510(k)	K924185	DFS GENIUS BTE	ESD	1992-11-03	View
510(k)	K905679	133 SERIES BTE	ESD	1991-01-28	View
510(k)	K905692	143 SERIES BTE	ESD	1991-01-28	View
510(k)	K896996	CAS (COMPUTERIZED ANALYZER SYSTEM)	ETW	1990-08-09	View
510(k)	K896995	DISCRETION, IN THE CANAL HEARING INSTRUMENT	ESD	1990-04-30	View
510(k)	K891594	CERUMEN FILTER	ESD	1989-05-10	View
510(k)	K863975	CUSTOM IN-THE-EAR	ESD	1986-11-07	View

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