FDA 510(k) Application Details - K963822

Device Classification Name	Hearing Aid, Air Conduction   More FDA Info for this Device
510(K) Number	K963822
Device Name	Hearing Aid, Air Conduction
Applicant	ORSONIQUE, INC. 4025 BOUL. INDUSTRIEL SUITE #100 LAVAL, QUEBEC H7L 4S3 CA Other 510(k) Applications for this Company
Contact	EUGENE ALEXANDRESCU Other 510(k) Applications for this Contact
Regulation Number	874.3300   More FDA Info for this Regulation Number
Classification Product Code	ESD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/23/1996
Decision Date	10/28/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review