Medical Device Manufacturer · US , St. Louis , MO

Koven and Assoc., Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1989

8

Total

8

Cleared

0

Denied

Koven and Assoc., Inc. has 8 FDA 510(k) cleared medical devices. Based in St. Louis, US.

Historical record: 8 cleared submissions from 1989 to 1993. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Koven and Assoc., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Koven and Assoc., Inc.

8 devices

1-8 of 8

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 Dec 10, 1992

MINI DOPPLER II ULTRASOUND BLOOD FLOW DETECTOR

Radiology · 365d

Cleared Mar 27, 1992

DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM

Cardiovascular · 227d

Cleared Dec 23, 1991

MODEL HD-207 BIDIRECTIONAL VELOCITY METER

Radiology · 206d

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