FDA 510(k)

BD Vacutainer® Multiple Sample Luer Adapter

K-Number: K243649 · 2025-03-21

Decision Date2025-03-21

Product CodeJKA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

BD Vacutainer® Multiple Sample Luer Adapter is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2025-03-21 under approval number K243649. 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® Multiple Sample Luer Adapter?

BD Vacutainer® Multiple Sample Luer Adapter is a medical device that received FDA 510(k) clearance on 2025-03-21. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K243649.

When was BD Vacutainer® Multiple Sample Luer Adapter approved by the FDA?

BD Vacutainer® Multiple Sample Luer Adapter received FDA 510(k) clearance on 2025-03-21, under approval number K243649.

What company makes BD Vacutainer® Multiple Sample Luer Adapter?

BD Vacutainer® Multiple Sample Luer Adapter is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Vacutainer® Multiple Sample Luer Adapter?

The FDA product code for BD Vacutainer® Multiple Sample Luer Adapter 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.