Data / Medical devices / United States / Becton, Dickinson & Co.

Becton, Dickinson & Co.: FDA-registered device maker in Cockeysville, MD, United States, 13 510(k) clearances

Name: Becton, Dickinson & Co. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Becton, Dickinson & Co. is registered with the FDA (registration 1111096) in Cockeysville, MD, United States. It lists 16 device types. The FDA files 13 510(k) clearances under its listings, the newest dated August 20, 2010. Registered through 2027. FDA data exported November 2, 2026.

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Get makers like this one Watch Becton, Dickinson & Co.

FDA registration number: 1111096
Address: 250 Schilling Cir, Cockeysville, MD, United States, 21030
Owner or operator: Becton Dickinson and Company (9922032)
Roles: Manufacturer
First device listed: December 29, 1977
Registered through: 2027
Brand names listed: 659611_BD Horizon Brilliant Stain Buffer, BBL CHROMagar Orientation, BD Alcohol Blend Rinse, BD BACTEC FOS Culture Supplement Kit, BD BACTEC MGIT 320, BD BACTEC MGIT 960, BD BACTEC MGIT 960 Calibration Vial, BD BACTEC MGIT 960 INH 0.4 Kit and more

Devices it lists

Device	Product code	Class	Role	Source
Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar	JSO	2	Manufacturer	accessdata.fda.gov
Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth	JTZ	2	Manufacturer	accessdata.fda.gov
Culture Media, Enriched	KZI	1	Manufacturer	accessdata.fda.gov
Culture Media, For Isolation Of Pathogenic Neisseria	JTY	2	Manufacturer	accessdata.fda.gov
Culture Media, General Nutrient Broth	JSC	1	Manufacturer	accessdata.fda.gov
Culture Media, Non-Selective And Differential	JSH	1	Manufacturer	accessdata.fda.gov
Culture Media, Non-Selective And Non-Differential	JSG	1	Manufacturer	accessdata.fda.gov
Culture Media, Selective And Differential	JSI	1	Manufacturer	accessdata.fda.gov
Culture Media, Selective And Non-Differential	JSJ	1	Manufacturer	accessdata.fda.gov
Culture Media, Selective Broth	JSD	1	Manufacturer	accessdata.fda.gov
Culture Media, Single Biochemical Test	JSF	1	Manufacturer	accessdata.fda.gov
General Purpose Reagent	PPM	1	Manufacturer	accessdata.fda.gov
Nephelometer, For Clinical Use	JQX	1	Manufacturer	accessdata.fda.gov
Susceptibility Test Powders, Antimycobacterial	MJA	2	Manufacturer	accessdata.fda.gov
System, Blood Culturing	MDB	1	Manufacturer	accessdata.fda.gov
System, Test, Automated, Antimicrobial Susceptibility, Short Incubation	LON	2	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
August 20, 2010	K092767	BBL CHROMAGAR MRSA II	JSO	Substantially Equivalent	Becton, Dickinson & CO	accessdata.fda.gov
November 20, 2007	K070691	BBL CHROMAGAR 0157	JSI	Substantially Equivalent	Becton, Dickinson & CO	accessdata.fda.gov
April 29, 2005	K050745	BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM, VANCOMYCIN (STREP) 0.0625 -32 UG/ML	LON	Substantially Equivalent	Becton, Dickinson & CO	accessdata.fda.gov
July 13, 2002	K021582	BACTEC MGIT 960 PZA KIT	MJA	Substantially Equivalent	Becton, Dickinson & CO	accessdata.fda.gov
May 23, 2002	K020321	BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM	LON	Substantially Equivalent	Becton, Dickinson & CO	accessdata.fda.gov
April 19, 2002	K014123	BACTEC MGIT 960 SIRE KITS	MJA	Substantially Equivalent	Becton, Dickinson & CO	accessdata.fda.gov
June 6, 2001	K003062	BACTEC MGIT 960 SIR KITS	MJA	Substantially Equivalent	Bd Becton Dickinson Vacutainer Systems Preanalytic	accessdata.fda.gov
May 1, 1998	K974883	BACTEC MGIT 960 SYSTEM	MDB	Substantially Equivalent	Bd Becton Dickinson Vacutainer Systems Preanalytic	accessdata.fda.gov
August 21, 1996	K954932	BBL MGIT PRODUCTS	MDB	Substantially Equivalent	Becton Dickinson Diagnostic Instrument Systems	accessdata.fda.gov
April 4, 1996	K960420	MUELLER HINTON AGAR WITH 5% SHEEP BLOOD	JTZ	Substantially Equivalent	Becton Dickinson Microbiology Systems	accessdata.fda.gov
April 17, 1992	K920933	BACTEC FOS CULTURE SUPPLEMENT	MDB	Substantially Equivalent	Bd Becton Dickinson Vacutainer Systems Preanalytic	accessdata.fda.gov
December 16, 1983	K833759	GROUP STREP BROTH T3472 LIM	JSD	Substantially Equivalent	Gibco Laboratories Life Technologies, Inc.	accessdata.fda.gov
October 7, 1976	K760588	IMPROVED THAYER MARTIN MEDIUM	JTY	Substantially Equivalent	Bd Becton Dickinson Vacutainer Systems Preanalytic	accessdata.fda.gov

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Updated August 20, 2010. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.