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. Radiology ✕
14 devices
Cleared
May 22, 2017
Pinpoint GT Needle Guide Kits
Radiology
14d
Cleared
Dec 14, 2015
Site-Rite 8 Ultrasound System, Site-Rite 8 Ultrasound System with Pinpoint GT...
Radiology
97d
Cleared
Mar 30, 2015
Site-Rite Prevue Ultrasound System, Site-Rite Prevue+ Ultrasound System
Radiology
28d
Cleared
Oct 30, 2014
Site-Rite 6 Ultrasound System with Pinpoint GT Technology
Radiology
58d
Cleared
May 02, 2014
BRACHYSOURCE SEED IMPLANTS WITH SOURCECAP BIOABSORBABLE CAPS
Radiology
29d
Cleared
Oct 17, 2013
SITE-RITE VISION II ULTRASOUND SYSTEM
Radiology
28d
Cleared
Dec 23, 2009
RADIONUCLIDE BRACHYTHERAPY SOURCE
Radiology
28d
Cleared
May 18, 2007
SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6
Radiology
17d
Cleared
Apr 19, 2006
PALLADIUM-103 SEED IMPLANT KITS -MULTIPLE
Radiology
40d
Cleared
Sep 29, 2005
SITE-RITE 5 ULTRASOUND SYSTEM
Radiology
15d
Cleared
Apr 18, 2005
SURE-POINT MIDLINE STEPPING AND STABILIZATION SYSTEM
Radiology
28d
Cleared
Feb 02, 2005
BRACHYSOURCE BRACHYTHERAPY SEED IMPLANTS
Radiology
71d