Data / Medical devices / United States / Becton, DIckinson and Company
Becton, DIckinson and Company: FDA-registered device maker in Canaan, CT, United States, 13 510(k) clearances
Becton, DIckinson and Company is registered with the FDA (registration 1213809) in Canaan, CT, United States. It lists 9 device types. The FDA files 13 510(k) clearances under its listings, the newest dated September 4, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1213809
- Address
- Route 7 And Grace Way, Canaan, CT, United States, 06018
- Owner or operator
- Becton Dickinson and Company (9922032)
- Roles
- Manufacturer
- First device listed
- August 3, 2001
- Registered through
- 2026
- Brand names listed
- BD 1mL Luer-Lok Hypodermic Syringe, BD 1mL Luer-Lok Hypodermic Syringe with BD Eclipse Hypodermic Needle, BD 1mL Luer-Lok Hypodermic Syringe with BD Hypodermic Needle, BD 1mL Luer-Lok Insulin Syringe, BD 1ml Insulin Syringe U-100 Luer-Lok Tip, BD 1ml Syringe Luer-Lok Tip, BD 1ml Syringe Luer-Lok Tip with BD PrecisionGlide Needle, BD Blunt Fill NRFit Needle and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Injection | FGY | 1 | Manufacturer | accessdata.fda.gov |
| Container, Liquid Medication, Graduated | KYW | 1 | Manufacturer | accessdata.fda.gov |
| Dispenser, Liquid Medication | KYX | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Aspiration And Injection, Disposable | GAA | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Manufacturer | accessdata.fda.gov |
| Piston Syringe With Neuraxial Connector Epidural, Peripheral, And/Or Indirect Cerebral Spinal Fluid Contact | QEH | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Antistick | MEG | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Manufacturer | accessdata.fda.gov |
| Tubes, Gastrointestinal (And Accessories) | KNT | 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 |
|---|---|---|---|---|---|---|
| September 4, 2020 | K192538 | BD Syringe NRFit Lok and BD Syringe NRFit Slip | QEH | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| December 19, 2016 | K162081 | BD 1ml Luer-lok Hypodermic Syringe, BD 1 mL Luer-Lok Hypodermic Syringe with BD Hypodermic Needle or BD Eclipse Hypodermic Needle, BD 1ml Luer-lok Insulin Syringe | FMF | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| September 29, 2011 | K112434 | BD ORAL/ENTERAL SYRINGE WITH BD UNIVIA CONNECTION | KNT | Substantially Equivalent | Bd Medical Surgical | accessdata.fda.gov |
| May 13, 2011 | K110771 | BD SINGLE USE, HYPODERMIC SYRINGE | FMF | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| June 13, 2001 | K011103 | BD SPRING BASED SYRINGE | MEG | Substantially Equivalent | Bd | accessdata.fda.gov |
| June 25, 1998 | K980580 | BECTON DICKINSON SYRINGES | FMF | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| June 11, 1998 | K980987 | BECTON DICKINSON SYRINGE | FMF | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| June 3, 1998 | K974363 | BECTON DICKINSON BLUNT PLASTIC CANNULA | FMI | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| January 22, 1998 | K974006 | BECTON DICKINSON TWINPAK | FMI | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| October 7, 1995 | K951254 | SAFETYGLIDE NEEDLE | FMI | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| May 26, 1994 | K941562 | 1ML LUER-LOK SYRINGE | FMF | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| February 12, 1993 | K924439 | BECTON DICKINSON INTERLINK VIAL ACCESS CANNULA | FMI | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| December 17, 1992 | K924072 | BECTON DICKINSON SAFETY-LOK SYRINGE | FMF | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Piston
- All makers of Syringe, Antistick
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Dispenser, Liquid Medication
- All makers of Tubes, Gastrointestinal (And Accessories)
- All makers of Needle, Aspiration And Injection, Disposable
Updated September 4, 2020. 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.