FDA 510(k) Application Details - K992291

Device Classification Name	Standard Polysomnograph With Electroencephalograph   More FDA Info for this Device
510(K) Number	K992291
Device Name	Standard Polysomnograph With Electroencephalograph
Applicant	GRASS-TELEFACTOR PRODUCT GROUP 1094 NEW DEHAVEN AVE. WEST CONSHOHOCKEN, PA 19428 US Other 510(k) Applications for this Company
Contact	JAMES S BRYAN Other 510(k) Applications for this Contact
Regulation Number	882.1400   More FDA Info for this Regulation Number
Classification Product Code	OLV Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/07/1999
Decision Date	08/06/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review