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510(k) Premarket Notification Database

Device Classification Name:	ACCELERATOR, LINEAR, MEDICAL
Regulation Number:	892.5050 [See Other Products with this regulation number]
510(k) Number:	K031764
Device Name:	ONCOR AVANT-GARDE WITH COHERENCE WORKSPACES
Applicant:	SIEMENS MEDICAL SOLUTIONS USA, INC. 4040 NELSON AVE. CONCORD, CA 94520
Contact:	KEN NEHMER
Product Code:	IYE [See Other Manufacturers that make this Product]
Date Received:	06-09-2003
Decision Date:	09-05-2003
Decision:	SE
Advisory Committee:	RA
Statement/Summary/Purged Status:	Summary
Type:	Traditional
Review by Third Party:	N
Expedited Review:	N

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