FDA 510(k) Application Details - K943224

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K943224
Device Name	Accelerator, Linear, Medical
Applicant	VARIAN ASSOC., INC. 911 HANSEN WAY PALO ALTO, CA 94303 US Other 510(k) Applications for this Company
Contact	CHARLES H WILL 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	07/05/1994
Decision Date	02/02/1996
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