Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1024879

FEI Number

1024879

Entity Name

BECTON, DICKINSON & CO., (BD)

City/State/Country

SUMTER, SC, US

Establishment Address

1575 Airport Rd, SUMTER, SC 29153, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Becton Dickinson and Company (Owner Number: 9922032)

Owner / Operator Contact Address

One Becton Drive, Franklin Lakes, NJ 07417, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K243649

PMA Number

N/A

All Registered Proprietary Names

BD BBL Venting Unit BD BACTEC Subculturing/Aerobic Venting Unit BD Vacutainer Urine Complete Cup Kit with Clot Activator BD Vacutainer Serum Tubes BD Vacutainer® Push Button UltraTouch Blood Collection Set BD Vacutainer® Push Button UltraTouch Blood Collection Set with Pre-Attached Holder BD Vacutainer® Plus Serum Tubes BD Vacutainer® Plus K2EDTA Tubes BD Vacutainer® SST¿ Glass Tubes BD Vacutainer® SST¿ II Advance Tubes BD Vacutainer® SST¿ Plus Tubes BD Vacutainer(R) Eclipse(TM) Blood Collection Needle with PreAttached Holder BD Vacutainer® Eclipse Blood Collection Needle BD Serum Separation Tubes BD Vacutainer SST Tubes BD Vacutainer® Multiple Sample Luer Adapter

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JTA	Monitor, Microbial Growth	Microbiology	Class 1	866.2560	2001-08-28
OIE	Urine Collection Kit (Excludes Hiv Testing)	Pathology	Class 1	864.3250	2025-12-17
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2008-01-07
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2022-04-06
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2022-04-06
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2007-12-26
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2025-07-16
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2008-01-07
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2025-03-26

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Becton Dickinson and Company

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
9680577	BECTON DICKINSON GMBH	HEIDELBERG Baden-Wurttemberg, DE
3003916417	BECTON DICKINSON IND. CIRURGICAS LTDA.	CURITIBA Parana, BR
3036495171	BD Biosciences San Diego	San Diego, CA, US
3015292643	BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES	San Diego, CA, US
3010141591	BD Kiestra B.V.	Drachten Fryslan, NL

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K945777	Smiths Industries Medical Systems, Inc.	PRO-VENT(TM), PULSATOR(R), AND LINE DRAW(TM) ARTERIAL BLOOD SAMPLING SYRINGES	1994-12-22
K221518	Np Medical	NP Medical nCompass Extension Set with Stabilizing Base	2022-11-03
K953474	Medikmark, Inc.	IV START KIT	1995-10-02
K972493	Nipro Medical Corp.	NIPRO DISPOSABLE SOLUTION INFUSION SET	1997-09-18
K982672	Baxter Healthcare Corp	COLLEAGUE PUMP SYRINGE ADAPTER SET	1998-09-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0022-2009	Becton Dickinson and Company	1	BD Visitec High Viscosity Injector, 4mm Ref: 585173. The product is intended for Vitroretinal Surgery.
Z-0030-2014	Perkin Elmer Health Sciences, Inc.	2	Perkin Elmer 226 Sample Collection Device, Serial numbers: 06132903 - 06198900. The PerkinElmer 226 Sample Collection Devices are intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory, in newborn screening. The device includes a tear-apart form for the collection of demographic information.
Z-0010-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, Product Code 21-7002-24
Z-0011-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24
Z-0012-2013	Baxter Healthcare Corp. Rt.	2	Baxter Interlink System Buretrol Solution Set with 150 mL Burette (Ball-Valve Drip Chamber); a sterile Rx IV fluid pathway device. Product Usage: The device is used for the administration of fluids from a container into the patient's vascular system through a vascular access device.

Similar Registrations

Registration Number	Establishment Name	Location
2022807	HARDY DIAGNOSTICS	Orcutt, CA, US
1950204	BIOMERIEUX, INC.	HAZELWOOD, MO, US
1119779	BECTON, DICKINSON & CO.	SPARKS, MD, US
1917413	BECTON, DICKINSON & CO.	BROKEN BOW, NE, US
1047843	ISOMEDIX OPERATIONS INC.	SPARTANBURG, SC, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1024879. Last updated year: 2026. Please use registration number 1024879 when referencing this establishment in official correspondence.