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FDA 510(k)

BD Veritor™ System Flu A+B Assay

K-Number: K133138 · 2013-11-13

ApplicantBecton, Dickinson & CO
Decision Date2013-11-13
Product CodePSZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BD Veritor™ System Flu A+B Assay is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson & CO. It received FDA 510(k) clearance on 2013-11-13 under 510(k) number K133138. The device is classified under product code PSZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD Veritor™ System Flu A+B Assay?

BD Veritor™ System Flu A+B Assay is a medical device that received FDA 510(k) clearance on 2013-11-13. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K133138.

When did BD Veritor™ System Flu A+B Assay receive FDA 510(k) clearance?

BD Veritor™ System Flu A+B Assay received FDA 510(k) clearance on 2013-11-13, under 510(k) number K133138.

Who is the listed applicant for BD Veritor™ System Flu A+B Assay?

The FDA 510(k) record lists Becton, Dickinson & CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD Veritor™ System Flu A+B Assay?

The FDA product code for BD Veritor™ System Flu A+B Assay is PSZ.

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Other records listing Becton, Dickinson & CO as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K160164BD Veritor System for Rapid Detection of Flu A + B Labratory KitK160161BD Veritor System for Rapid Detection of Flu A + B CLIA waived kitK133140BD VERITOR SYSTEM FOR THE RAPID DETECTION OF RSVK130268BD PROBETEC TRICHOMONAS VAGINALIS (TV) QX AMPLIFIED DNA ASSAYK131301BD FACS SAMPLE PREP ASSISTANT IIIK131358BD PEN NEEDLE

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Related Devices (Code: PSZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254262Sofia Influenza A+B FIA; Sofia RSV FIA; Sofia Strep A+ FIAOrtho Clinical Diagnostics Inc. (QuidelOrtho)K252283Nano-Check Influenza A+B TestNano-Ditech CorporationK250398Innovita Flu A/B Antigen Rapid TestInnovita (Tangshan) Biological Technology Co., Ltd.K241188Acucy® Influenza A&B Test with the Acucy® 2 SystemSEKISUI Diagnostics, LLCK232434BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived KitBdK223016BD VeritorTM System for Rapid Detection of Flu A+B CLIA-Waived KitBd

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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