FDA 510(k) Application Details - K070920

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K070920
Device Name	Accelerator, Linear, Medical
Applicant	FUJIFILM MEDICAL SYSTEMS U.S.A., INC. 419 WEST AVE. STAMFORD, CT 06902-6300 US Other 510(k) Applications for this Company
Contact	DEBBIE PEACOCK 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	04/02/2007
Decision Date	05/22/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review