Bard Interventional Products Div. - FDA 510(k) Cleared Devices
Recent clearances: BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES, BARD HIGH FLOW PAPILLOTOME
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bard Interventional Products Div. Gastroenterology & Urology ✕
2 devices