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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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