Akers Laboratories, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Akers Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HEALTHTEST HEPARIN/PLATELET FACTOR 4 ANTIBODY ASSAY, INSTAREAD LITHIUM SYSTEM, AKERS LABORATORIES INC. BLOOD CELL SEPARATOR
3
Total
3
Cleared
0
Denied
Akers Laboratories, Inc. has 3 FDA 510(k) cleared medical devices. Based in Thorofare, US.
Historical record: 3 cleared submissions from 2003 to 2004.
Browse the FDA 510(k) cleared devices submitted by Akers Laboratories, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Akers Laboratories, Inc.
3 devices