FDA 510(k) Applications Submitted by KOVEN TECHNOLOGY, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K131623 06/04/2013 SMARTDOP XT KOVEN TECHNOLOGY, INC.
K201114 04/27/2020 Bidop 7 Koven Technology, Inc.
K143332 11/20/2014 Fast Sphyg by Koven KOVEN TECHNOLOGY, INC.
K153762 12/30/2015 Smartdop XT6 KOVEN TECHNOLOGY, INC.
K080178 01/24/2008 VALVULOTOME BY KOVEN KOVEN TECHNOLOGY, INC.
K010452 02/15/2001 BI-DIRECTIONAL DOPPLER VOLUME FLOWMETER, MODEL DVM-4300 & 4300T KOVEN TECHNOLOGY, INC.
K050601 03/09/2005 SMARTDOP 45 VASCULAR DOPPLER KOVEN TECHNOLOGY, INC.
K031504 05/14/2003 ECHO SOUNDER, SINGLE-HANDED, MODEL ES-101EX KOVEN TECHNOLOGY, INC.
K031931 06/23/2003 ECHO SOUNDER EX-101EX 8 MHZ KOVEN TECHNOLOGY, INC.
K023143 09/20/2002 ECHO SOUNDER, ES-102EX KOVEN TECHNOLOGY, INC.
K951449 03/29/1995 MODEL KM-25 KOVEN TECHNOLOGY, INC.
K961817 05/10/1996 B SMART MODEL 1 KOVEN TECHNOLOGY, INC.
K963274 08/20/1996 V-LINK 3.2 FOR WINDOWS KOVEN TECHNOLOGY, INC.
K982986 08/26/1998 TUBING BLOOD FLOW METER MODEL NUMBER HD-800 KOVEN TECHNOLOGY, INC.
K954397 09/20/1995 BIDIRECTIONAL DOPPLER W/WAVEFORM DISPLAY KOVEN TECHNOLOGY, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact