FDA 510(k) Application Details - K070676

Device Classification Name	Apparatus, Vestibular Analysis   More FDA Info for this Device
510(K) Number	K070676
Device Name	Apparatus, Vestibular Analysis
Applicant	SPORTKAT, LLC 1497 POINSETTIA AVE. STE. 157 VISTA, CA 92083 US Other 510(k) Applications for this Company
Contact	DAMON R LAWSON Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LXV Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/12/2007
Decision Date	04/18/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review