Bracco Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bracco Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HeartSee™ Cardiac P.E.T. Processing Software For Myocardial Perfusion and Coronary Flow Reserve (CFR) Version 4, HeartSee Cardiac P.E.T. Processing Software
2
Total
2
Cleared
0
Denied
Bracco Diagnostics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Monroe Township, US.
Latest FDA clearance: Mar 2025. Active since 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Bracco Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bracco Diagnostics, Inc.
2 devices