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FDA 510(k)

BD Vacutainer® Citrate Blood Collection Tubes

K-Number: K240455 · 2024-10-31

ApplicantBecton, Dickinson and Company
Decision Date2024-10-31
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BD Vacutainer® Citrate Blood Collection Tubes is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2024-10-31 under approval number K240455. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD Vacutainer® Citrate Blood Collection Tubes?

BD Vacutainer® Citrate Blood Collection Tubes is a medical device that received FDA 510(k) clearance on 2024-10-31. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K240455.

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

BD Vacutainer® Citrate Blood Collection Tubes received FDA 510(k) clearance on 2024-10-31, under approval number K240455.

What company makes BD Vacutainer® Citrate Blood Collection Tubes?

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

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

The FDA product code for BD Vacutainer® Citrate Blood Collection Tubes is GIM.

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Related Devices (Code: GIM)

K162723TransFix/EDTA Vacuum Blood Collection TubesCaltag Medsystems, Ltd. K230493BD MiniDraw Capillary Blood Collection System with BD MiniDraw H&H Capillary Blood Collection TubeBecton, Dickinson and Company K213670BD Vacutainer K2EDTA Blood Collection Tubes, BD Vacutainer K3EDTA Blood Collection TubesBecton, Dickinson and Company

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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