FDA 510(k) Applications Submitted by DAVID DUERSTELER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K030199	01/21/2003	GE MOBILE DISCOVERY ST PET CT IMAGING SYSTEM	GENERAL ELECTRIC CO.
K970901	03/11/1997	GE LOGIQ 500 DIAGNOSTIC ULTRASOUND SYSTEM	GE MEDICAL SYSTEMS
K141074	04/25/2014	CORTEX ID SUITE	GE MEDICAL SYSTEMS, LLC
K041220	05/10/2004	GE DISCOVERY ST SYSTEM	GE MEDICAL SYSTEMS
K081496	05/29/2008	OPTIMA PET/CT 560	GE MEDICAL SYSTEMS, LLC
K041922	07/16/2004	GE TETHERED PORTABLE DIGITAL RADIOGRAPHIC DETECTOR	GENERAL ELECTRIC CO.
K042257	08/20/2004	DISCOVERY ST PET/CT IMAGING SYSTEM WITH AN ALTERNATE DETECTOR OPTION	GENERAL ELECTRIC CO.
K022872	08/29/2002	GE ROAD WARRIOR PET CT IMAGING SYSTEM	GENERAL ELECTRIC CO.
K964617	10/28/1996	GE LOGIQ 700 DIAGNOSTIC ULTRASOUND SYSTEM	GE MEDICAL SYSTEMS
K113408	11/18/2011	Q. FREEZE (MOTION VUE2)	GE MEDICAL SYSTEMS, LLC
K133657	11/27/2013	DISCOVERY PET/CT 710	GE MEDICAL SYSTEMS, LLC
K964886	12/06/1996	GE LOGIQ 700 DIAGNOSTIC ULTRASOUND SYSTEM	GE MEDICAL SYSTEMS