FDA 510(k) Application Details - K110932

Device Classification Name	Masker, Tinnitus   More FDA Info for this Device
510(K) Number	K110932
Device Name	Masker, Tinnitus
Applicant	GN RESOUND A/S LAUTRUPBJERG 7 BALLERUP 2750 DK Other 510(k) Applications for this Company
Contact	LARS HAGANDER Other 510(k) Applications for this Contact
Regulation Number	874.3400   More FDA Info for this Regulation Number
Classification Product Code	KLW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/04/2011
Decision Date	05/03/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review