C.R. Bard, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220), BD Touchless™ Plus Unisex Pre-Lubricated Urethral Catheter Kit, Elyra™ Thulium Fiber Laser System and Elyra™ Plus Thulium Fiber Laser System (Laser, Fibers, and Accessories)
646
Total
610
Cleared
0
Denied
FDA 510(k) Regulatory Record - C.R. Bard, Inc. Toxicology ✕
1 devices