FDA 510(k) Application Details - K012306

Device Classification Name	Calibrator, Hearing Aid / Earphone And Analysis Systems   More FDA Info for this Device
510(K) Number	K012306
Device Name	Calibrator, Hearing Aid / Earphone And Analysis Systems
Applicant	ETYMONIC DESIGN, INC. 41 BYRON AVE. DORCHESTER, ONTARIO NOL 1GO CA Other 510(k) Applications for this Company
Contact	WILLIAM A COLE Other 510(k) Applications for this Contact
Regulation Number	874.3310   More FDA Info for this Regulation Number
Classification Product Code	ETW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/23/2001
Decision Date	09/21/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review