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FDA 510(k)

BD Vacutainer Eclipse UltraFill Blood Collection Needle

K-Number: K181730 · 2019-03-01

ApplicantBecton, Dickinson and Company
Decision Date2019-03-01
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BD Vacutainer Eclipse UltraFill Blood Collection Needle is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2019-03-01 under approval number K181730. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD Vacutainer Eclipse UltraFill Blood Collection Needle?

BD Vacutainer Eclipse UltraFill Blood Collection Needle is a medical device that received FDA 510(k) clearance on 2019-03-01. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K181730.

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

BD Vacutainer Eclipse UltraFill Blood Collection Needle received FDA 510(k) clearance on 2019-03-01, under approval number K181730.

What company makes BD Vacutainer Eclipse UltraFill Blood Collection Needle?

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

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

The FDA product code for BD Vacutainer Eclipse UltraFill Blood Collection Needle is FMI.

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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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