Bard Medical Div. is one of 15076 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bard Medical Div. - FDA 510(k) Cleared Devices
Recent clearances: BARDEX LUBRI-SIL I.C. FOLEY CATHETER, BARDEX LUBRI-SIL FOLEY CATHETER, BARD FLEXIBLE ENDOSCOPY INJECTION SYSTEM (651019)
3
Total
3
Cleared
0
Denied
Bard Medical Div. has 3 FDA 510(k) cleared medical devices. Based in Covington, US.
Historical record: 3 cleared submissions from 1997 to 1999. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Bard Medical Div. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bard Medical Div.
3 devices