Koven Technology, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Koven Technology, Inc. has 18 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Last cleared in 2021. Active since 1994. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Koven Technology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Delphi Consulting Group as regulatory consultant.
FDA 510(k) Regulatory Record - Koven Technology, Inc.
18 devices
Cleared
Jan 05, 2021
Bidop 7
Cardiovascular
253d
Cleared
May 25, 2016
Smartdop XT6
Cardiovascular
147d
Cleared
Apr 14, 2015
Fast Sphyg by Koven
Cardiovascular
145d
Cleared
Jan 17, 2014
SMARTDOP XT
Cardiovascular
227d
Cleared
Jul 28, 2008
VALVULOTOME BY KOVEN
Cardiovascular
186d
Cleared
Apr 15, 2005
SMARTDOP 45 VASCULAR DOPPLER
Radiology
37d
Cleared
Feb 13, 2004
ECHO SOUNDER EX-101EX 8 MHZ
Cardiovascular
235d
Cleared
Jul 18, 2003
ECHO SOUNDER, SINGLE-HANDED, MODEL ES-101EX
Radiology
65d
Cleared
Dec 19, 2002
ECHO SOUNDER, ES-102EX
Radiology
90d
Cleared
Feb 12, 2002
BI-DIRECTIONAL DOPPLER VOLUME FLOWMETER, MODEL DVM-4300 & 4300T
Cardiovascular
362d
Cleared
Nov 24, 1998
TUBING BLOOD FLOW METER MODEL NUMBER HD-800
Radiology
90d
Cleared
Jul 23, 1997
B SMART MODEL 1
Neurology
439d