Koven Technology, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
FDA 510(k) cleared devices by Koven Technology, Inc. Radiology ✕
9 devices
Cleared
Apr 15, 2005
SMARTDOP 45 VASCULAR DOPPLER
Radiology
37d
Cleared
Jul 18, 2003
ECHO SOUNDER, SINGLE-HANDED, MODEL ES-101EX
Radiology
65d
Cleared
Dec 19, 2002
ECHO SOUNDER, ES-102EX
Radiology
90d
Cleared
Nov 24, 1998
TUBING BLOOD FLOW METER MODEL NUMBER HD-800
Radiology
90d
Cleared
Oct 31, 1996
V-LINK 3.2 FOR WINDOWS
Radiology
72d
Cleared
May 20, 1996
MODEL KM-25
Radiology
418d
Cleared
Mar 29, 1996
BIDIRECTIONAL DOPPLER W/WAVEFORM DISPLAY
Radiology
191d
Cleared
May 11, 1995
PW DOPPLER VASCULAR PROBES
Radiology
512d
Cleared
Dec 23, 1994
SMARTDOP 30 BI-DIRECTIONAL BLOOD FLOW DETECTOR
Radiology
204d