FDA 510(k) Applications Submitted by TESSA YAMUT

FDA 510(k) Number Submission Date Device Name Applicant
K030141 01/15/2003 MODIFICATION TO CARDIOVENTION POWERBASE CONSOLE, MODEL PCB-100 CARDIOVENTION, INC.
K021694 05/22/2002 CARDIOVENTION POWERBASE CONSOLE, MODEL PBC-100 CARDIOVENTION, INC.
K032068 07/03/2003 CARDIOVENTION CORX IOS-200 SYSTEM, MODEL IOS-200 CARDIOVENTION, INC.
K012325 07/23/2001 CARDIOVENTION CORX SYSTEM, MODEL FG 0001 CARDIOVENTION, INC.


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