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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:	K032156
Device Name:	ACCUFIX RADIOLUCENT PELVIS AND BELLY BOARDS, ACCUFIX CANTILEVER HEAD BOARD WITH SHOULDER DEPRESSION, ACCUFIX RADIOLUCENT
Applicant:	WFR/AQUAPLAST CORP. 30 LAWLINS PARK WYCKOFF, NJ 07481
Contact:	J. DAMON KIRK
Product Code:	IYE [See Other Manufacturers that make this Product]
Date Received:	07-15-2003
Decision Date:	09-02-2003
Decision:	SE
Advisory Committee:	RA
Statement/Summary/Purged Status:	Statement
Type:	Traditional
Review by Third Party:	N
Expedited Review:	N

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