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FDA 510(k)

BD Vacutainer® One Use Holder

K-Number: K242320 · 2024-11-01

ApplicantBecton, Dickinson and Company
Decision Date2024-11-01
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BD Vacutainer® One Use Holder is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2024-11-01 under approval number K242320. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD Vacutainer® One Use Holder?

BD Vacutainer® One Use Holder is a medical device that received FDA 510(k) clearance on 2024-11-01. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K242320.

When was BD Vacutainer® One Use Holder approved by the FDA?

BD Vacutainer® One Use Holder received FDA 510(k) clearance on 2024-11-01, under approval number K242320.

What company makes BD Vacutainer® One Use Holder?

BD Vacutainer® One Use Holder is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Vacutainer® One Use Holder?

The FDA product code for BD Vacutainer® One Use Holder is JKA.

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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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