FDA 510(k) Applications Submitted by KENNETH D BUROKER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K970224	01/21/1997	PIXI BONE DENSITOMETER	LUNAR CORP.
K060912	04/03/2006	MODIFICATION TO: HI-ART SYSTEM	TOMOTHERAPY INCORPORATED
K982267	06/29/1998	DPX-RX BONE DENSITOMETER	LUNAR CORP.
K972517	07/07/1997	EXPERT-XL ORTHOPEDIC HIP ACQUISITION AND ANALYSIS SOFTWARE	LUNAR CORP.
K983262	09/17/1998	FRACTURE RISK ASSESSMENT OPTION FOR PIXI BONE DENSITOMETERS	LUNAR CORP.
K983269	09/17/1998	FRACTURE RISK ASSESSMENT OPTION FOR EXPERT-XL BONE DENSITOMETER	LUNAR CORP.
K983271	09/17/1998	FRACTURE RISK ASSESSMENT OPTION FOR DPX SERIES BONE DENSITOMETERS	LUNAR CORP.
K042739	10/04/2004	HI-ART SYSTEM	TOMOTHERAPY INCORPORATED
K983564	10/13/1998	PRODIGY TOTAL BODY SOFTWARE	LUNAR CORP.
K033347	10/20/2003	MODIFICATION TO: HI-ART SYSTEM	TOMOTHERAPY INCORPORATED
K983724	10/22/1998	ORCA-DX BONE DENSITOMETER	LUNAR CORP.
K964263	10/25/1996	EXPERT-KL AND HAND ACQUISITION AND ANALYSIS SOFTWARE	LUNAR CORP.
K964307	10/29/1996	EXPANDED REFERENCE VALUES FOR DPX BON DENSITOMETERS	LUNAR CORP.
K013673	11/06/2001	HI-ART SYSTEM	TOMO THERAPY INC
K974437	11/24/1997	EXPERT-XL LATERAL SPINE BMD ACQUISITION AND ANALYSIS SOFTWARE	LUNAR CORP.
K965226	12/30/1996	EXPERT-XL TOTAL BODY ACQUISITION AND ANALYSIS SOFTWARE	LUNAR CORP.