Data / Medical devices / United States / Becton Dickinson And Company
Becton Dickinson And Company: FDA-registered device maker in Columbus, NE, United States, 17 510(k) clearances
Becton Dickinson And Company is registered with the FDA (registration 1911916) in Columbus, NE, United States. It lists 17 device types. The FDA files 17 510(k) clearances under its listings, the newest dated July 16, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1911916
- Address
- 2153 12th Ave, Columbus, NE, United States, 68601
- Owner or operator
- Becton Dickinson and Company (9922032)
- Roles
- Contract sterilizer, Manufacturer, Repackager or relabeler
- First device listed
- August 3, 2001
- Registered through
- 2026
- Brand names listed
- Alcohol Swab, BD Blunt Fill NRFit Needle, BD Blunt Fill Needle, BD Blunt Filter NRFit Needle, BD Blunt Filter Needle, BD Catheter Tip Syringe, BD Hypodermic Needles, BD Hypodermic Syringe and more
Devices it lists
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 |
|---|---|---|---|---|---|---|
| July 16, 2022 | K213955 | 0.9% Sodium Chloride Injection, USP, BD PosiFlush SafeScrub | QTI | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| November 9, 2020 | K193190 | BD PureHub Disinfecting Cap | QBP | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| September 4, 2020 | K192538 | BD Syringe NRFit Lok and BD Syringe NRFit Slip | QEH | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| February 27, 2017 | K163591 | BD PosiFlush Heparin Lock Flush Syringe | NZW | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| February 2, 2017 | K161552 | 0.9% Sodium Chloride Injection, USP BD PosiFlush SP Syringe | NGT | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| July 25, 2014 | K141311 | 0.9% SODIUM CHLORIDE INJECTION, USP BD POSIFLUSH; SP SYRINGE, SF SYRINGE | NGT | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| March 20, 2013 | K121655 | BD ALCOHOL SWAB | LKB | Substantially Equivalent | Becton, Dickinson & CO | 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 10, 2009 | K090680 | HEPARIN LOCK FLUSH SOLUTION, USP BD POSIFLUSH HEPARIN LOCK FLUSH SYRINGE | NZW | Substantially Equivalent | Becton, Dickinson & CO | accessdata.fda.gov |
| July 19, 2002 | K021475 | BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SET | FMI | Substantially Equivalent | Bd | accessdata.fda.gov |
| June 13, 2001 | K011103 | BD SPRING BASED SYRINGE | MEG | Substantially Equivalent | Bd | 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 |
| February 12, 1993 | K924439 | BECTON DICKINSON INTERLINK VIAL ACCESS CANNULA | FMI | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
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Updated July 16, 2022. 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.