Medical Device Manufacturer · US , Franklin Lakes , NJ

Becton Dickinson

6 submissions · 6 cleared · Since 2004
6
Total
6
Cleared
0
Denied

Becton Dickinson — FDA 510(k) Submissions

Becton Dickinson has submitted 6 FDA 510(k) premarket notifications since 2004, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Blood Culturing, Glucose Oxidase, Glucose, Saline, Vascular Access Flush, Syringe, Piston, Infusion Safety Management Software . Use the specialty filter in the sidebar to narrow results.

6 devices
1–6 of 6
BD Intelliport System; BD Intelliport Reader (516230); BD Intelliport Sensor (516229); BD Intelliport Gateway (516232); BD Intelliport Mount (516233); BD Intelliport Charger (516231)
K243062 · PHC Infusion Safety... · General Hospital
Jun 2025 266d
BD BACTEC Standard/10 Aerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial
K161810 · MDB System, Blood Culturing · Microbiology
Feb 2017 223d
BD BACTEC Standard Anaerobic/F Culture Vials Soybean-Casein Digest Broth in a Plastic Vial
K161306 · MDB System, Blood Culturing · Microbiology
Aug 2016 90d
BD EMERALD SINGLE USE, HYPODERMIC SYRINGE
K113241 · FMF Syringe, Piston · General Hospital
Nov 2011 26d
BD LOGIC BLOOD GLUCOSE MONITOR AND PARADIGM LINK BLOOD GLUCOSE MONITOR
K041478 · CGA Glucose Oxidase, Glucose · Chemistry
Oct 2004 147d
0.9% SODIUM CHLORIDE INJECTION, USP BD POSTFLUSH SF FLUSH SYRINGE
K042061 · NGT Saline, Vascular Access... · General Hospital
Aug 2004 24d
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