Becton, Dickinson and Company (Bard Access Systems, Inc.) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Becton, Dickinson and Company (Bard Access Systems, Inc.) - FDA 510(k...
Recent clearances: PowerGlide Pro™ Midline Catheter
1
Total
1
Cleared
0
Denied
Becton, Dickinson and Company (Bard Access Systems, Inc.) has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Latest FDA clearance: Jul 2024. Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Becton, Dickinson and Company (Bard Access Systems, Inc.) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Becton, Dickinson and Company (Bard Access Systems, Inc.)
1 devices