FDA 510(k) Application Details - K151207

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K151207
Device Name	Accelerator, Linear, Medical
Applicant	ORFIT INDUSTRIES NV VOSVELD 9A WIJNEGEM B-2110 BE Other 510(k) Applications for this Company
Contact	EDDY MARIVOET Other 510(k) Applications for this Contact
Regulation Number	892.5050   More FDA Info for this Regulation Number
Classification Product Code	IYE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/06/2015
Decision Date	07/28/2015
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review