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FDA 510(k)

BD CTGCTV2

K-Number: K210585 · 2022-05-10

ApplicantBecton, Dickinson and Company
Decision Date2022-05-10
Product CodeQEP
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BD CTGCTV2 is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2022-05-10 under 510(k) number K210585. The device is classified under product code QEP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD CTGCTV2?

BD CTGCTV2 is a medical device that received FDA 510(k) clearance on 2022-05-10. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K210585.

When did BD CTGCTV2 receive FDA 510(k) clearance?

BD CTGCTV2 received FDA 510(k) clearance on 2022-05-10, under 510(k) number K210585.

Who is the listed applicant for BD CTGCTV2?

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

What is the FDA product code for BD CTGCTV2?

The FDA product code for BD CTGCTV2 is QEP.

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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.

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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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