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FDA 510(k)

BD Vacutainer® Fluoride Blood Collection Tubes

K-Number: K231237 · 2024-01-19

ApplicantBecton, Dickinson and Company
Decision Date2024-01-19
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BD Vacutainer® Fluoride Blood Collection Tubes is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2024-01-19 under approval number K231237. 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® Fluoride Blood Collection Tubes?

BD Vacutainer® Fluoride Blood Collection Tubes is a medical device that received FDA 510(k) clearance on 2024-01-19. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K231237.

When was BD Vacutainer® Fluoride Blood Collection Tubes approved by the FDA?

BD Vacutainer® Fluoride Blood Collection Tubes received FDA 510(k) clearance on 2024-01-19, under approval number K231237.

What company makes BD Vacutainer® Fluoride Blood Collection Tubes?

BD Vacutainer® Fluoride Blood Collection Tubes is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Vacutainer® Fluoride Blood Collection Tubes?

The FDA product code for BD Vacutainer® Fluoride Blood Collection Tubes 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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