FDA 510(k) Applications Submitted by STEVEN J KACHELMEYER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K110798	03/22/2011	SENOGRAPHE DS, SENOGRAPHE ESSENTIAL	GENERAL ELECTRIC COMPANY
K082104	07/25/2008	GE LIGHTSPEED RT16 / LIGHTSPEED XTRA V2 CT SYSTEM (AKA GE LIGHTSPEED RT16 / LIGHTSPEED XTRA CT SYSTEM	GE MEDICAL SYSTEMS, INC.
K082816	09/25/2008	GE BRIGHTSPEED DELIGHT CT SCANNER SYSTEM	GE MEDICAL SYSTEMS, LLC
K082960	10/03/2008	GE XTREME INJECTOR OPTION	GE MEDICAL SYSTEMS, LLC
K103485	11/26/2010	SENOGRAPH DS, SENOGRAPH ESSENSTIAL	GENERAL ELECTRIC COMPANY
K013381	10/12/2001	ADVANCED LUNG ANALYSIS-1	GENERAL ELECTRIC CO.
K013422	10/15/2001	CARDIQ FUNCTION	GE MEDICAL SYSTEMS