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FDA 510(k)

BD Vacutainer UltraTouch Push Button Blood Collection Set

K-Number: K153309 · 2016-02-12

ApplicantBecton, Dickinson and Company
Decision Date2016-02-12
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BD Vacutainer UltraTouch Push Button Blood Collection Set is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2016-02-12 under approval number K153309. 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 UltraTouch Push Button Blood Collection Set?

BD Vacutainer UltraTouch Push Button Blood Collection Set is a medical device that received FDA 510(k) clearance on 2016-02-12. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K153309.

When was BD Vacutainer UltraTouch Push Button Blood Collection Set approved by the FDA?

BD Vacutainer UltraTouch Push Button Blood Collection Set received FDA 510(k) clearance on 2016-02-12, under approval number K153309.

What company makes BD Vacutainer UltraTouch Push Button Blood Collection Set?

BD Vacutainer UltraTouch Push Button Blood Collection Set is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Vacutainer UltraTouch Push Button Blood Collection Set?

The FDA product code for BD Vacutainer UltraTouch Push Button Blood Collection Set is JKA.

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Related Devices (Code: 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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