Diadexus, Inc. is one of 14102 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diadexus, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PLAC TEST FOR LP-PLA2 ACTIVITY, PLAC TEST REAGENT KIT,CALIBRATOR KIT, LP-PLA2 CONTROL KIT, MODEL(S) 90107,90109,90109, MODIFICATION TO DIADEXUS PLAC TEST
7
Total
7
Cleared
0
Denied
Diadexus, Inc. has 7 FDA 510(k) cleared medical devices. Based in South San Francisco, US.
Historical record: 7 cleared submissions from 2003 to 2014. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Diadexus, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diadexus, Inc.
7 devices
Cleared
Dec 15, 2014
PLAC TEST FOR LP-PLA2 ACTIVITY
Chemistry
186d
Cleared
Jan 03, 2011
PLAC TEST REAGENT KIT, MODELS 90107, 90112, 90115, 90116, 10-0112, 10-0113,...
Chemistry
186d
Cleared
Dec 20, 2007
PLAC TEST REAGENT KIT,CALIBRATOR KIT, LP-PLA2 CONTROL KIT, MODEL(S)...
Chemistry
97d
Cleared
Sep 11, 2006
MODIFICATION TO DIADEXUS PLAC TEST
Chemistry
40d
Cleared
Jun 15, 2005
DIADEXUS PLAC TEST
Chemistry
105d
Cleared
Feb 05, 2004
MODIFICATION TO DIADEXUS PLAC TEST
Chemistry
16d
Cleared
Jul 18, 2003
DIADEXUS PLAC TEST
Chemistry
155d