Becton Dickinson - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Becton Dickinson has 6 FDA 510(k) cleared medical devices. Based in Franklin Lakes, US.
Latest FDA clearance: Jun 2025. Active since 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Becton Dickinson Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Becton Dickinson
6 devices
Cleared
Jun 20, 2025
BD Intelliport System
General Hospital
266d
Cleared
Feb 09, 2017
BD BACTEC Standard/10 Aerobic/F Culture Vials Soybean-Casein Digest Broth in...
Microbiology
223d
Cleared
Aug 08, 2016
BD BACTEC Standard Anaerobic/F Culture Vials Soybean-Casein Digest Broth in a...
Microbiology
90d
Cleared
Nov 28, 2011
BD EMERALD SINGLE USE, HYPODERMIC SYRINGE
General Hospital
26d
Cleared
Oct 28, 2004
BD LOGIC BLOOD GLUCOSE MONITOR AND PARADIGM LINK BLOOD GLUCOSE MONITOR
Chemistry
147d
Cleared
Aug 26, 2004
0.9% SODIUM CHLORIDE INJECTION, USP BD POSTFLUSH SF FLUSH SYRINGE
General Hospital
24d