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

FDA 510(k) Number Submission Date Device Name Applicant
K110256 01/28/2011 THE IC-PRO SYSTEM PAIEON, INC.
K113594 12/05/2011 C-THV SYSTEM PAIEON, INC.
K030139 01/14/2003 THE CARDIOP-B SYSTEM PAIEON, INC.
K072591 09/14/2007 CARDIOP-B SYSTEM, VERSION 2.1 PAIEON, INC.
K073328 11/27/2007 CARDIOP-B SYSTEM, VERSION 2.1 WITH LVA PAIEON, INC.
K082907 09/30/2008 IC-PRO SYSTEM, VERSION 3.1.0.4 PAIEON, INC.
K083745 12/16/2008 THE IC-PRO SYSTEM, MODEL VERSION 3.2 PAIEON, INC.
K120282 01/31/2012 CARDNAV PAIEON, INC.


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