Sonosite,Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sonosite,Inc. - FDA 510(k) Cleared Devices
Recent clearances: SONOSITE EDGE ULTRASOUND SYSTEM, BIO Z CARDIO PROFILE HEMODYNAMIC MONITOR, SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM
23
Total
23
Cleared
0
Denied
Sonosite,Inc. has 23 FDA 510(k) cleared radiology devices. Based in Bothell, US.
Historical record: 23 cleared submissions from 1998 to 2011.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC, Tuv Product Service, Inc. and Tuv America, Inc..
FDA 510(k) Regulatory Record - Sonosite,Inc.
23 devices
Cleared
Nov 15, 2011
SONOSITE EDGE ULTRASOUND SYSTEM
Radiology
20d
Cleared
Jun 03, 2011
BIO Z CARDIO PROFILE HEMODYNAMIC MONITOR
Cardiovascular
91d
Cleared
Nov 19, 2010
SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM
Radiology
88d
Cleared
Aug 23, 2010
LUMENVU CATHETER GUIDANCE SYSTEM
General Hospital
284d
Cleared
Aug 12, 2010
SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM, SONOSITE MAXX SERIES ULTRASOUND...
Radiology
50d
Cleared
Oct 02, 2009
SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM
Radiology
86d
Cleared
Aug 25, 2008
SONOSITE MAXX SERIES ULTRASOUND SYSTEM
Radiology
31d
Cleared
May 08, 2007
SONOSITE MAXX SERIES DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
15d
Cleared
Nov 16, 2005
SONOSITE MICROMAXX DIAGNOSTIC ULTRASOUND SYSTEM (C3 SERIES)
Radiology
15d
Cleared
Aug 11, 2005
SONOSITE HAND-CARRIED ULTRASOUND SYSTEM (C1 SERIES)
Radiology
7d
Cleared
Jan 12, 2005
SONOSITE HIGH-RESOLUTION DIAGNOSTIC ULTRASOUND SYSTEM (C3 SERIES)
Radiology
16d
Cleared
Dec 21, 2004
TITAN HIGH RESOLUTION ULTRASOUND SYSTEM AND SONOSITE ULTRASOUND SYSTEM
Radiology
6d