Ultrasonix Medical Corporation is one of 570 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Ultrasonix Medical Corporation - FDA 510(k) Cleared Devices
Recent clearances: SONIXGPS, SONIXGPS NEEDLE SENSOR, SONIXTABLET ULTRASOUND SCANNER
11
Total
11
Cleared
0
Denied
Ultrasonix Medical Corporation has 11 FDA 510(k) cleared radiology devices. Based in Vancouver, Bc, CA.
Historical record: 11 cleared submissions from 2002 to 2013.
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 and Intertek Testing Services.
FDA 510(k) Regulatory Record - Ultrasonix Medical Corporation
11 devices
Cleared
Dec 02, 2013
SONIXGPS
Anesthesiology
530d
Cleared
Jun 13, 2012
SONIXGPS NEEDLE SENSOR
Radiology
351d
Cleared
Jan 25, 2012
SONIXTABLET ULTRASOUND SCANNER
Radiology
43d
Cleared
Sep 27, 2011
SONIX ULTRASOUND SCANNER
Radiology
7d
Cleared
Dec 21, 2010
SONIXTABLET ULTRASOUND SCANNER
Radiology
75d
Cleared
Nov 20, 2009
SONIX ULTRASOUND SCANNER
Radiology
14d
Cleared
Oct 31, 2008
SONIXTOUCH ULTRASOUND SYSTEM
Radiology
14d
Cleared
Aug 06, 2008
SONIX MDP ULTRASOUND SCANNER
Radiology
126d
Cleared
Aug 04, 2006
SONIX ULTRASOUND SCANNER
Radiology
37d
Cleared
Sep 16, 2004
ERGOSONIX ULTRASOUND SCANNER, MODULO ULTRASOUND SCANNER
Radiology
20d
Cleared
Jun 13, 2002
ULTRASONIX ERGOSONIX 500 ULTRASOUND SCANNER
Radiology
107d