FDA 510(k) Applications Submitted by HITACHI MEDICAL CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K061608	06/09/2006	MODIFICATION TO EUB-5500 DIAGNOSTIC ULTRASOUND SCANNER	HITACHI MEDICAL CORP.
K053258	11/22/2005	EUB-6500 DIAGNOSTIC ULTRASOUND SCANNER	HITACHI MEDICAL CORP.
K042501	09/14/2004	ETG-4000 OPTICAL TOPOGRAPHY SYSTEM	HITACHI MEDICAL CORP.
K073310	11/23/2007	OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL	HITACHI MEDICAL CORP.
K011252	04/24/2001	EUB-6000 DIAGNOSTIC ULTRASOUND SCANNER SP-711 SONOPROBE SYSTEM	HITACHI MEDICAL CORP.
K012239	07/17/2001	MODIFICATIONS TO EUB-525 DIAGNOSTIC ULTRASOUND SCANNER; EUB-2000 DIAGNOSTIC ULTRASOUND SCANNER; SP-711 SONOPROBE SYSTEM	HITACHI MEDICAL CORP.
K013722	11/09/2001	MODIFICATION TO: EUB-8500 DIAGNOSTIC ULTRASOUND SCANNER	HITACHI MEDICAL CORP.
K013723	11/09/2001	MODIFICATION TO: EUB-6500 DIAGNOSTIC ULTRASOUND SCANNER	HITACHI MEDICAL CORP.