ClearanceBrief
Company ยท US

Advanced Vascular Dynamics

FDA 510(k) clearances and medical device recalls filed under this name, 2004 to 2015. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DXCClamp, Vascular6
JOMPlethysmograph, Photoelectric, Pneumatic Or Hydraulic1
KKXDrape, Surgical, Antimicrobial1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 31, 2015K151363Zephyr Vascular Compression Device
Advanced Vascular Dynamics
DXC
Dec 4, 2014K142122RADAR VASCULAR COMPRESSION DEVICE
Advanced Vascular Dynamics
DXC
Jan 31, 2014K131571AVD RIGHT RADIAL DRAPE
Advanced Vascular Dynamics
KKX
Feb 12, 2010K093192FLOCHEC PHOTO PLETHYSMOGRAPHIC DEVICE
Advanced Vascular Dynamics
JOM
Nov 19, 2009K092503RADAR VASCULAR COMPRESSION DEVICES
Advanced Vascular Dynamics
DXC
Mar 23, 2009K090286PRESSUREMATE MANUAL FEMORAL ACCESS COMPRESSION DEVICE
Advanced Vascular Dynamics
DXC
Sep 6, 2007K072167COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE
Advanced Vascular Dynamics
DXC
Jun 1, 2004K040615COMPRESSAR SUPERCOMFORT DISC AND STRONGARM SUPERCOMFORT SYSTEM
Advanced Vascular Dynamics
DXC

Latest recalls

DateFirm and productCodeLinked 510(k)
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