Medical Device Manufacturer · US , St. Louis , MO

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

18 submissions · 18 cleared · Since 1994

Total

Cleared

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.

FDA 510(k) cleared devices by Koven Technology, Inc.

18 devices

1-12 of 18

Cleared Jan 05, 2021

Bidop 7

K201114 · DPW

Cardiovascular · 253d

Cleared May 25, 2016

Smartdop XT6

K153762 · JOP

Cardiovascular · 147d

Cleared Apr 14, 2015

Fast Sphyg by Koven

K143332 · DXQ

Cardiovascular · 145d

Cleared Jan 17, 2014

SMARTDOP XT

K131623 · JOP

Cardiovascular · 227d

Cleared Jul 28, 2008

VALVULOTOME BY KOVEN

K080178 · MGZ

Cardiovascular · 186d

Cleared Apr 15, 2005

SMARTDOP 45 VASCULAR DOPPLER

K050601 · DPW

Radiology · 37d

Cleared Feb 13, 2004

ECHO SOUNDER EX-101EX 8 MHZ

K031931 · DPW

Cardiovascular · 235d

Cleared Jul 18, 2003

ECHO SOUNDER, SINGLE-HANDED, MODEL ES-101EX

K031504 · KNG

Radiology · 65d

Cleared Dec 19, 2002

ECHO SOUNDER, ES-102EX

K023143 · KNG

Radiology · 90d

Cleared Feb 12, 2002

BI-DIRECTIONAL DOPPLER VOLUME FLOWMETER, MODEL DVM-4300 & 4300T

K010452 · DPW

Cardiovascular · 362d

Cleared Nov 24, 1998

TUBING BLOOD FLOW METER MODEL NUMBER HD-800

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

FDA 510(k) cleared devices by Koven Technology, Inc.

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