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FDA 510(k) Applications Submitted by JAMES 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.
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