Akers Biosciences, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Akers Biosciences, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Akers Biosciences, Inc. has 5 FDA 510(k) cleared medical devices. Based in Thorofare, US.
Historical record: 5 cleared submissions from 2005 to 2011. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Akers Biosciences, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Akers Biosciences, Inc.
5 devices
Cleared
Jan 12, 2011
BREATHSCN PRO
Toxicology
147d
Cleared
Dec 18, 2006
BREATH ALCOHOL CHECK .02 AND BREATHSCAN .02 DETECTION SYSTEMS
Toxicology
80d
Cleared
Apr 28, 2006
BREATHSCAN, BREATH AND BREATH CHECK ALCOHOL DETECTORS
Toxicology
38d
Cleared
Jan 04, 2006
HEPARIN/PLATELET FACTOR 4 ANTIBODY SERUM PANEL
Hematology
98d
Cleared
Mar 04, 2005
MODIFICATION TO: INSTAREAD LITHIUM SYSTEM
Chemistry
21d