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FDA 510(k)

BD Vacutainer® Eclipse™ Blood Collection Needle

K-Number: K243207 · 2025-07-03

ApplicantBecton, Dickinson and Company
Decision Date2025-07-03
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BD Vacutainer® Eclipse™ Blood Collection Needle is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2025-07-03 under approval number K243207. 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® Eclipse™ Blood Collection Needle?

BD Vacutainer® Eclipse™ Blood Collection Needle is a medical device that received FDA 510(k) clearance on 2025-07-03. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K243207.

When was BD Vacutainer® Eclipse™ Blood Collection Needle approved by the FDA?

BD Vacutainer® Eclipse™ Blood Collection Needle received FDA 510(k) clearance on 2025-07-03, under approval number K243207.

What company makes BD Vacutainer® Eclipse™ Blood Collection Needle?

BD Vacutainer® Eclipse™ Blood Collection Needle is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Vacutainer® Eclipse™ Blood Collection Needle?

The FDA product code for BD Vacutainer® Eclipse™ Blood Collection Needle 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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