Sonosite,Inc.

FDA 510(k) & PMA Approved Devices — 23 products

Total Devices23

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K113156	SONOSITE EDGE ULTRASOUND SYSTEM	IYO	2011-11-15	View
510(k)	K110645	BIO Z CARDIO PROFILE HEMODYNAMIC MONITOR	DSB	2011-06-03	View
510(k)	K102390	SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM	IYN	2010-11-19	View
510(k)	K093510	LUMENVU CATHETER GUIDANCE SYSTEM	OMF	2010-08-23	View
510(k)	K101757	SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM, SONOSITE MAXX SERIES ULTRASOUND SYSTEM	ITX	2010-08-12	View
510(k)	K092058	SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM	IYN	2009-10-02	View
510(k)	K082098	SONOSITE MAXX SERIES ULTRASOUND SYSTEM	IYN	2008-08-25	View
510(k)	K071134	SONOSITE MAXX SERIES DIAGNOSTIC ULTRASOUND SYSTEM	IYO	2007-05-08	View
510(k)	K053069	SONOSITE MICROMAXX DIAGNOSTIC ULTRASOUND SYSTEM (C3 SERIES)	IYN	2005-11-16	View
510(k)	K052109	SONOSITE HAND-CARRIED ULTRASOUND SYSTEM (C1 SERIES)	IYN	2005-08-11	View
510(k)	K043559	SONOSITE HIGH-RESOLUTION DIAGNOSTIC ULTRASOUND SYSTEM (C3 SERIES)	IYN	2005-01-12	View
510(k)	K043452	TITAN HIGH RESOLUTION ULTRASOUND SYSTEM AND SONOSITE ULTRASOUND SYSTEM	IYN	2004-12-21	View
510(k)	K033367	TITAN ULTRASOUND SYSTEM, SONOSITE ILOOK 25 ULTRASOUND SYSTEM, 180PLUS ULTRASOUND SYSTEM, MODEL L03073, L02245, L02464	IYN	2003-11-05	View
510(k)	K030949	TITAN HIGH RESOLUTION ULTRASOUND SYSTEM	IYN	2003-04-07	View
510(k)	K030064	ILOOK 25 NEEDLE GUIDE ATTACHMENT AND BRACKET ASSEMBLY	ITX	2003-01-22	View
510(k)	K023957	SONOSITE HAND-CARRIED ULTRASOUND SYSTEM (C2 SERIES)	IYN	2002-12-12	View
510(k)	K021628	SONOSITE HAND-CARIED UNTRASOUND SYSTEM (POWERSERIES)	IYN	2002-05-31	View
510(k)	K014116	HAND-CARRIED ULTRASOUND SYSTEM	IYN	2001-12-20	View
510(k)	K010374	SONOSITE HAND-CARRIED ULTRASOUND SYSTEM	IYN	2001-02-21	View
510(k)	K003399	SONOSITE HAND-CARRIED ULTRASOUND SYSTEM	IYN	2000-11-16	View