Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BD Vacutainer® Citrate Blood Collection Tubes

K-Number: K240455 · 2024-10-31

Decision Date2024-10-31
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BD Vacutainer® Citrate Blood Collection Tubes is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2024-10-31 under 510(k) 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. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K240455.

When did BD Vacutainer® Citrate Blood Collection Tubes receive FDA 510(k) clearance?

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

Who is the listed applicant for BD Vacutainer® Citrate Blood Collection Tubes?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

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.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Becton, Dickinson and Company as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 100 devices →

Related Devices (Code: GIM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.