Koven and Assoc., Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
6 devices
Cleared
Jan 29, 1993
MULTIDOP MODEL HD-2020 BI-DIRECTIONAL BLOOD FLOW
Cardiovascular
239d
Cleared
Jan 22, 1993
SMARTDOP 20 BI-DIRECTIONAL BLOOD FLOW DETECTOR
Cardiovascular
361d
Cleared
Mar 27, 1992
DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM
Cardiovascular
227d
Cleared
Feb 26, 1991
ES-1000SP II SMART DOP
Cardiovascular
231d
Cleared
Oct 27, 1989
HD-2200 PNEUMO-DOP VASCULAR TESTING SYSTEM
Cardiovascular
87d
Cleared
Jul 28, 1989
DVM-4200 BLOOD FLOWMETER
Cardiovascular
105d