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FDA 510(k)

BD VERITOR SYSTEM FOR THE RAPID DETECTION OF RSV

K-Number: K133140 · 2013-11-15

Decision Date2013-11-15
Product CodeGQG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BD VERITOR SYSTEM FOR THE RAPID DETECTION OF RSV 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 2013-11-15 under 510(k) number K133140. The device is classified under product code GQG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD VERITOR SYSTEM FOR THE RAPID DETECTION OF RSV?

BD VERITOR SYSTEM FOR THE RAPID DETECTION OF RSV is a medical device that received FDA 510(k) clearance on 2013-11-15. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K133140.

When did BD VERITOR SYSTEM FOR THE RAPID DETECTION OF RSV receive FDA 510(k) clearance?

BD VERITOR SYSTEM FOR THE RAPID DETECTION OF RSV received FDA 510(k) clearance on 2013-11-15, under 510(k) number K133140.

Who is the listed applicant for BD VERITOR SYSTEM FOR THE RAPID DETECTION OF RSV?

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 FOR THE RAPID DETECTION OF RSV?

The FDA product code for BD VERITOR SYSTEM FOR THE RAPID DETECTION OF RSV is GQG.

Related Clinical Trials

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.

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.

View all 190 devices →

Related Devices (Code: GQG)

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.

Official Source

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

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