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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