Abbott Laboratories, Inc. is one of 16539 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Abbott Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ARCHITECT IVALPROIC ACID REAGENTS AND ARCHITECT IVALPROIC ACID CALIBRATORS, MODELS 1P35, 1P35, CREATININE, PRECISION XTRA PLUS OR OPTIUM PLUS, BLOOD GLUCOSE TEST STRIPS
6
Total
6
Cleared
0
Denied
Abbott Laboratories, Inc. has 6 FDA 510(k) cleared medical devices. Based in Abbott Park, US.
Historical record: 6 cleared submissions from 2002 to 2009. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Abbott Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Abbott Laboratories, Inc.
6 devices
Cleared
Aug 06, 2009
ARCHITECT IVALPROIC ACID REAGENTS AND ARCHITECT IVALPROIC ACID CALIBRATORS,...
Chemistry
175d
Cleared
Jun 23, 2006
CREATININE
Chemistry
56d
Cleared
May 27, 2005
PRECISION XTRA PLUS OR OPTIUM PLUS, BLOOD GLUCOSE TEST STRIPS
Chemistry
15d
Cleared
May 11, 2004
FOX PLUS PTA CATHETER
Cardiovascular
28d
Cleared
Apr 30, 2004
AXSYM CYCLOSPORINE
Chemistry
36d
Cleared
Sep 30, 2002
GEMSTAR INFUSION PUMP SYSTEM, 7 THERAPY, 6 THERAPY & PAIN MANAGEMENT
General Hospital
14d