Data / Medical devices / United States / Becton, Dickinson & Co.
Becton, Dickinson & Co.: FDA-registered device maker in Broken Bow, NE, United States, 19 510(k) clearances
Becton, Dickinson & Co. is registered with the FDA (registration 1917413) in Broken Bow, NE, United States. It lists 13 device types. The FDA files 19 510(k) clearances under its listings, the newest dated March 13, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1917413
- Address
- 150 S 1st Ave, Broken Bow, NE, United States, 68822
- Owner or operator
- Becton Dickinson and Company (9922032)
- Roles
- Contract sterilizer, Manufacturer
- First device listed
- September 13, 1994
- Registered through
- 2026
- Brand names listed
- BD BACTEC Subculturing/Aerobic Venting Unit, BD BBL Venting Unit, BD Blunt Fill NRFit Needle, BD Blunt Fill Needle, BD Blunt Filter NRFit Needle, BD Blunt Filter Needle, BD CPT Tube with Sodium Heparin, BD INTERLINK CANNULA SYSTEMS and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood/Plasma Collection Device For Dna Testing | PJE | 2 | Manufacturer | accessdata.fda.gov |
| Cannula, Injection | FGY | 1 | Manufacturer | accessdata.fda.gov |
| Container, Specimen Mailer And Storage, Sterile | KDT | 1 | Manufacturer | accessdata.fda.gov |
| Container, Specimen, Sterile | FMH | 1 | Manufacturer | accessdata.fda.gov |
| Culture Media, Non-Propagating Transport | JSM | 1 | Manufacturer | accessdata.fda.gov |
| Lymphocyte Separation Medium | JCF | 1 | Manufacturer | accessdata.fda.gov |
| Monitor, Microbial Growth | JTA | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Aspiration And Injection, Disposable | GAA | 1 | Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Contract sterilizer | accessdata.fda.gov |
| System, Transport, Aerobic | JTW | 1 | Manufacturer | accessdata.fda.gov |
| Tubes, Vacuum Sample, With Anticoagulant | GIM | 2 | Manufacturer | accessdata.fda.gov |
| Tubes, Vials, Systems, Serum Separators, Blood Collection | JKA | 2 | Manufacturer | accessdata.fda.gov |
| Urine Collection Kit (Excludes Hiv Testing) | OIE | 1 | 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 |
|---|---|---|---|---|---|---|
| March 13, 2026 | K252040 | BD Vacutainer® Plasma Separator Tubes (PST), BD Vacutainer® Sodium Heparin Blood Collection Tubes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| November 1, 2024 | K242320 | BD Vacutainer® One Use Holder | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| February 2, 2024 | K231373 | BD Vacutainer® K2 EDTA Blood Collection Tubes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| January 19, 2024 | K231237 | BD Vacutainer® Fluoride Blood Collection Tubes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| August 25, 2023 | K213670 | BD Vacutainer K2EDTA Blood Collection Tubes, BD Vacutainer K3EDTA Blood Collection Tubes | GIM | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| July 17, 2023 | K213953 | BD Vacutainer® Trace Element K2EDTA Tubes, BD Vacutainer® Trace Element Serum Tubes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| January 21, 2010 | K093972 | BD MICROTAINER MAP MICROTUBE FOR AUTOMATED PROCESS, MODEL 363706 | JKA | Substantially Equivalent | Becton, Dickinson & CO | accessdata.fda.gov |
| May 14, 2004 | K041071 | BD VACUTAINER TRACE ELEMENT SERUM PLUS TUBE AND BD VACUTAINER TRACE ELEMENT K2EDTA PLUS TUBE, MODELS 368380/368381 | JKA | Substantially Equivalent | Becton, Dickinson & CO | accessdata.fda.gov |
| March 26, 2003 | K024240 | BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS | JSM | Substantially Equivalent | Bd | accessdata.fda.gov |
| February 1, 2002 | K013971 | BD VACUTAINER SAFETY COAGULATION TUBE | JKA | Substantially Equivalent | Becton, Dickinson & CO | accessdata.fda.gov |
| June 17, 1998 | K981013 | VACUTAINER PLUS TUBE WITH EDTA ANTICOAGULANT ANDD VACUTAINER PLUS SERUM TUBE | JKA | Substantially Equivalent for Some Indications | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
| February 24, 1998 | K972075 | VACUTAINER BRAND PPT PLASMA PREPARATION TUBE | PJE | Substantially Equivalent | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
| March 29, 1996 | K960250 | VACUTAINER BRAND PLUS SERUM & SST TUBES | JKA | Substantially Equivalent | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
| November 28, 1995 | K954592 | VACUTAINER BRAND PST PLASMA SEPARATION TUBE | JKA | Substantially Equivalent | Becton Dickinson Vacutainer Systems | accessdata.fda.gov |
| November 10, 1994 | K944566 | VACUTAINER BRAND PLUS SODIUM HEPARIN TUBE | JKA | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| December 15, 1992 | K911731 | LEUCOPREP(R) BRAND CELL SEPARAT TUBE W/SODIUM CITR | JCF | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| August 9, 1990 | K901449 | VACUTAINER PLUS WITH HEMOGARD CLOSURE | JKA | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| May 26, 1989 | K891407 | LEUCOPREP CELL SEPARATION TUBE | JCF | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| April 4, 1979 | K790366 | URINE CULTURE KIT | JTW | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
Compare with other makers
- All makers of Lymphocyte Separation Medium
- All makers of Cannula, Injection
- All makers of Tubes, Vials, Systems, Serum Separators, Blood Collection
- All makers of System, Transport, Aerobic
- All makers of Culture Media, Non-Propagating Transport
- All makers of Tubes, Vacuum Sample, With Anticoagulant
Updated March 13, 2026. 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.