FDA 510(k) Applications Submitted by SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI

FDA 510(k) Number	Submission Date	Device Name	Applicant
K163289	11/22/2016	syngo. CT Single Source Dual Energy (twin beam)	SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
K072090	07/30/2007	SIEMENS DIAGNOSTIC ULTRASOUND SYSTEMS	SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
K080760	03/18/2008	ACUSON X300 ULTRASOUND SYSTEM	SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
K071036	04/12/2007	MODIFICATION TO ACUSON X300 ULTRASOUND SYSTEM	SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
K081121	04/21/2008	MODIFICATION TO ACUSON X150 ULTRASOUND SYSTEM	SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
K063803	12/22/2006	ACUSON ANTARES DIAGNOSTIC ULTRASOUND SYSTEM	SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
K072365	08/23/2007	SEQUOIA PLUS DIAGNOSTIC ULTRASOUND SYSTEM	SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
K113179	10/28/2011	ACUSON SC2000 DIAGNOSTIC ULTRASOUND SYSTEM	SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
K081148	04/22/2008	SIEMENS ACUSON 2000 ULTRASOUND SYSTEM WITH ABVS TRANSDUCER	SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
K082142	07/30/2008	ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM	SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
K112596	09/07/2011	ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM	SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI