FDA 510(k) Application Details - K092117

Device Classification Name	More FDA Info for this Device
510(K) Number	K092117
Device Name	SCENAR, MODEL 10
Applicant	RITM OKB ZAO 99, PETROVSKAYA TAGANROG 347900 RU Other 510(k) Applications for this Company
Contact	LARISA SHPUNGINA Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/14/2009
Decision Date	05/28/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review