Bard Access Systems, Inc. - FDA 510(k) Cleared Devices
21
Total
20
Cleared
0
Denied
Bard Access Systems, Inc. has 20 FDA 510(k) cleared general hospital devices. Based in Salt Lake City, US.
Latest FDA clearance: Sep 2025. Active since 1993.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bard Access Systems, Inc.
21 devices
Cleared
Sep 05, 2025
Vaccess™ CT Low-Profile Power-Injectable Implantable Port
General Hospital
29d
Cleared
Jun 18, 2025
PowerPort™ isp Implantable Port
General Hospital
56d
Cleared
Nov 27, 2024
PowerLoc™ Max Power Injectable Infusion Set
General Hospital
198d
Cleared
Oct 31, 2024
PowerPort™ ClearVUE™ Slim Implantable Ports and PowerPort™ ClearVUE™ Slim...
General Hospital
86d
Cleared
Feb 18, 2024
BD Prevue™ II Peripheral Vascular Access System
Radiology
30d
Cleared
Aug 24, 2022
Sherlock 3CG® Tip Positioning System (TPS) Stylet/T-Lock Assembly
General Hospital
30d
Cleared
Jul 30, 2021
BD PowerPiCC Catheter
General Hospital
179d
Cleared
May 30, 2012
SITE RITE PREVUE ULTRASOUND SYSTEM AND PINPOINT NEEDLE GUIDE
Radiology
68d
Cleared
Mar 05, 2010
SITE-RITE VISION ULTRASOUND SYSTEM
Radiology
17d
Cleared
May 18, 2007
ASPIRA PLEURAL DRAINAGE SYSTEM
Anesthesiology
30d
Cleared
Apr 13, 2006
LONG-TERM HEMODIALYSIS CATHETERS WITH BIOBLOC COATING
Gastroenterology & Urology
111d
Cleared
Jan 13, 2006
POWERPICC
General Hospital
28d