C.R. Bard, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 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), Rubber Utility Catheter
645
Total
609
Cleared
0
Denied
FDA 510(k) Regulatory Record - C.R. Bard, Inc. ✕
1 devices