Last synced on 25 January 2026 at 3:41 am

BD VeritorTM System for Rapid Detection of Flu A+B CLIA-Waived Kit

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223016
510(k) Type
Traditional
Applicant
Bd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2023
Days to Decision
120 days
Submission Type
Summary

BD VeritorTM System for Rapid Detection of Flu A+B CLIA-Waived Kit

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223016
510(k) Type
Traditional
Applicant
Bd
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2023
Days to Decision
120 days
Submission Type
Summary