Advanced Vascular Dynamics is one of 5053 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Vascular Dynamics - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Advanced Vascular Dynamics has 8 FDA 510(k) cleared medical devices. Based in Portland, US.
Historical record: 8 cleared submissions from 2004 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Advanced Vascular Dynamics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Advanced Vascular Dynamics
8 devices
Cleared
Jul 31, 2015
Zephyr Vascular Compression Device
Cardiovascular
71d
Cleared
Dec 04, 2014
RADAR VASCULAR COMPRESSION DEVICE
Cardiovascular
122d
Cleared
Jan 31, 2014
AVD RIGHT RADIAL DRAPE
General Hospital
246d
Cleared
Feb 12, 2010
FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE
Cardiovascular
126d
Cleared
Nov 19, 2009
RADAR VASCULAR COMPRESSION DEVICES
Cardiovascular
97d
Cleared
Mar 23, 2009
PRESSUREMATE MANUAL FEMORAL ACCESS COMPRESSION DEVICE
Cardiovascular
46d
Cleared
Sep 06, 2007
COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE
Cardiovascular
31d
Cleared
Jun 01, 2004
COMPRESSAR SUPERCOMFORT DISC AND STRONGARM SUPERCOMFORT SYSTEM
Cardiovascular
84d