FDA 510(k) Application Details - K961817

Device Classification Name	Device, Sleep Assessment   More FDA Info for this Device
510(K) Number	K961817
Device Name	Device, Sleep Assessment
Applicant	KOVEN TECHNOLOGY, INC. 300 BROOKES DR. SUITE 105 ST. LOUIS, MO 63042 US Other 510(k) Applications for this Company
Contact	PAUL G KOVEN Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LEL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/10/1996
Decision Date	07/23/1997
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