Argus Cognitive, Inc. is one of 16321 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Argus Cognitive, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Neurora, ReVISION 2, Argus Cognitive ReVISION Software
3
Total
3
Cleared
0
Denied
Argus Cognitive, Inc. has 3 FDA 510(k) cleared medical devices. Based in Lebanon, US.
Latest FDA clearance: Oct 2026. Active since 2023. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Argus Cognitive, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Argus Cognitive, Inc.
3 devices