FDA 510(k) Application Details - K003644

Device Classification Name	Nystagmograph   More FDA Info for this Device
510(K) Number	K003644
Device Name	Nystagmograph
Applicant	EYETECT, L.L.C. 10 MADONNA COURT BELLEVILLE,, IL 62223 US Other 510(k) Applications for this Company
Contact	REBECCA M CUETO 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	11/27/2000
Decision Date	02/01/2001
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