FDA 510(k) Applications Submitted by JAMES P RASKOB

FDA 510(k) Number	Submission Date	Device Name	Applicant
K151570	06/10/2015	Carestation 620/650/650C	DATEX-OHMEDA, INC.
K122445	08/10/2012	AESPIRE 7900, AESPIRE VIEW	DATEX-OHMEDA
K072664	09/20/2007	GE LUNAR FEMUR STRENGTH SOFTWARE	GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA
K000826	03/14/2000	PRODIGY LATERAL VIEW SOFTWARE	LUNAR CORP.
K030962	03/27/2003	DPX SERIES BRAVO DUO BONE DENSITOMETER	GE LUNAR CORP.
K071570	06/08/2007	GE LUNAR BODY COMPOSITION SOFTWARE	GE MEDICAL SYSTEMS LUNAR
K001756	06/09/2000	LUNAR REPORT GENERATOR II	LUNAR CORP.
K001812	06/15/2000	PEDIATRIC REFERENCE DATA	LUNAR CORP.
K011917	06/20/2001	ADVANCED HIP ASSESSMENT SOFTWARE	GE LUNAR CORP.
K131945	06/27/2013	GE DATEX-OHMEDA AVANCE CS2	DATEX-OHMEDA
K132530	08/12/2013	GE DATEX-OHMEDA AISYS CS2 (AISYS CS^2)	DATEX-OHMEDA, INC.
K082317	08/13/2008	GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTION	GENERAL ELECTRIC CO.
K072439	08/30/2007	GE LUNAR DPX & PRODIGY SERIES DEXA BONE DENSITOMETERS WITH MOBILE KIT	GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA
K052581	09/20/2005	LUNAR IDXA	GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA
K123125	10/04/2012	GE DATEX-OHMEDA AVANCE CS2	DATEX-OHMEDA, INC.
K023554	10/23/2002	DUAL-ENERGY VERTEBRAL ASSESSMENT VIEW SOFTWARE	GE LUNAR CORP.