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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 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 2025-03-21 under 510(k) 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. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K243649.

When did BD Vacutainer® Multiple Sample Luer Adapter receive FDA 510(k) clearance?

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

Who is the listed applicant for BD Vacutainer® Multiple Sample Luer Adapter?

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 Vacutainer® Multiple Sample Luer Adapter?

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

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 and Company 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.

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Related Devices (Code: JKA)

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.