Abk Biomedical, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Abk Biomedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Easi-Vue® embolic microspheres System, Easi-Vue embolic microspheres System
2
Total
2
Cleared
0
Denied
Abk Biomedical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Halifax, CA.
Latest FDA clearance: Feb 2024. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Abk Biomedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Abk Biomedical, Inc.
2 devices