FDA 510(k) Application Details - K011181

Device Classification Name	Audiometer   More FDA Info for this Device
510(K) Number	K011181
Device Name	Audiometer
Applicant	ICS MEDICAL CORP. 125 COMMERCE DR. SCHAUMBURG, IL 60173-5329 US Other 510(k) Applications for this Company
Contact	DELMAR F BLOEM Other 510(k) Applications for this Contact
Regulation Number	874.1050   More FDA Info for this Regulation Number
Classification Product Code	EWO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/18/2001
Decision Date	06/25/2001
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