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FDA 510(k) Applications Submitted by CARDIOVENTION, INC.
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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