FDA 510(k) Applications Submitted by ROBERT L WOLFERT

FDA 510(k) Number Submission Date Device Name Applicant
K072599 09/14/2007 PLAC TEST REAGENT KIT,CALIBRATOR KIT, LP-PLA2 CONTROL KIT, MODEL(S) 90107,90109,90109 DIADEXUS, INC.
K040101 01/20/2004 MODIFICATION TO DIADEXUS PLAC TEST DIADEXUS, INC.
K030477 02/13/2003 DIADEXUS PLAC TEST DIADEXUS, INC.
K062234 08/02/2006 MODIFICATION TO DIADEXUS PLAC TEST DIADEXUS, INC.


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