FDA 510(k) Application Details - K013060

Device Classification Name	Nystagmograph   More FDA Info for this Device
510(K) Number	K013060
Device Name	Nystagmograph
Applicant	ICS MEDICAL 125 COMMERCE DR. SCHAUMBURG, IL 60173-5329 US Other 510(k) Applications for this Company
Contact	ROBERT M SIMENSON Other 510(k) Applications for this Contact
Regulation Number	882.1460   More FDA Info for this Regulation Number
Classification Product Code	GWN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/11/2001
Decision Date	12/10/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review