FDA Registration Active 🇺🇸 United States

BECTON, DICKINSON & CO.

Reg #: 3007886372 · FEI: 3007886372 · Expires 2026
Products
6
Proprietary Names
13
Establishment Types
1
Classifications
6

Registration Details

Registration Name
BECTON, DICKINSON & CO.
Registration Number
3007886372
FEI Number
3007886372
Status
Active
Expiry Year
2026
Initial Importer
No
Address
3750 Torrey View Ct
City
San Diego
State
CA
ZIP
92130
Country
US

Regulatory Submissions

510(k) Number
K160164

Owner / Operator

Firm Name
Becton Dickinson and Company
Operator Number
9922032
Address
One Becton Drive
City
Franklin Lakes
State
NJ
Postal Code
07417
Country
US

Products

Device Name Product Code
Devices Detecting Influenza A, B, And C Virus Antigens PSZ
Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus GQG
Simple Point-Of-Care Device To Directly Detect Sars-Cov-2 Viral Targets From Clinical Specimens In Near-Patient Settings QVF
Single (Specified) Analyte Controls (Assayed And Unassayed) JJX
Antigens, All Groups, Streptococcus Spp. GTY
Covid-19 Multi-Analyte Antigen Device QMN

Proprietary Names

BD Veritor™ System For Rapid Detection of Flu A+B Laboratory kit BD Veritor™ System For Rapid Detection of Flu A+B CLIA-waived kit BD Veritor™ System For Rapid Detection of RSV - Laboratory kit BD Veritor™ System for Rapid Detection of SARS-CoV-2 BD Veritor™ System Group A Strep Control Swab set BD Veritor™ System RSV Control Swab Set BD Veritor™ System Flu A+B Control Swab Set BD Veritor™ SARS-CoV-2 Control Swab Set BD Veritor™ System for Rapid Detection of Flu A+B CLIA-waived kit BD Veritor™ System for Rapid Detection of Group A Strep CLIA-Waived Kit BD Veritor™ System for Rapid Detection of SARS-CoV-2 & Flu A+B BD Veritor™ SARS-CoV-2 & Flu A+B Control Swab Set BD Veritor™ System For Rapid Detection of RSV - CLIA waived kit

Establishment Types

Develop Specifications But Do Not Manufacture At This Facility