FDA 510(k)

BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube

K-Number: K160657 · 2016-09-23

Decision Date2016-09-23

Product CodeJKA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2016-09-23 under approval number K160657. 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 Barricor Lithium Heparin Plasma Blood Collection Tube?

BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube is a medical device that received FDA 510(k) clearance on 2016-09-23. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K160657.

When was BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube approved by the FDA?

BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube received FDA 510(k) clearance on 2016-09-23, under approval number K160657.

What company makes BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube?

BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube?

The FDA product code for BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube 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.