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. 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
Cleared
Jul 02, 2004
SOURCELINK
Radiology
21d
Cleared
Nov 09, 1976
BARIMEX, BARIUM SULFATE COMPOUND
Radiology
42d