FDA 510(k) Applications Submitted by LOURDES COBA

FDA 510(k) Number Submission Date Device Name Applicant
K030291 01/28/2003 COULTER ACT 5DIFF AUTOLOADER (AL) BECKMAN COULTER, INC.
K100607 03/03/2010 COULTER 4C-EX 300 CELL CONTROL BECKMAN COULTER, INC.
K021150 04/10/2002 COULTER CELLPREP BECKMAN COULTER, INC.
K071681 06/19/2007 CYTOMICS FC 500 MPL FLOW CYTOMETER, MODEL # 626554 BECKMAN COULTER, INC.
K081822 06/27/2008 COULTER 6C CELL CONTROL, MODELS 628027 & A59925 BECKMAN COULTER, INC.
K032013 06/30/2003 COULTER ACT 5DIFF AL HEMATOLOGY ANALYZER BECKMAN COULTER, INC.
K081930 07/07/2008 UNICEL DXH 800 COULTER CELLULAR ANALYSIS SYSTEM BECKMAN COULTER, INC.
K082162 07/31/2008 COULTER BODY FLUID CONTROL BECKMAN COULTER, INC.
K042173 08/11/2004 COULTER A T 5DIFF CAP PIERCE (CP) BECKMAN COULTER, INC.
K013842 11/20/2001 IMMUNO-TROL LOW CELLS BECKMAN COULTER, INC.
K100790 03/22/2010 COULTER LIN-X LINEARITY CONTROL, MODEL A81196 BECKMAN COULTER, INC.


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