BD Vacutainer® K2 EDTA Blood Collection Tubes
K-Number: K231373 · 2024-02-02
Device Summary
Frequently Asked Questions
What is the BD Vacutainer® K2 EDTA Blood Collection Tubes?
BD Vacutainer® K2 EDTA Blood Collection Tubes is a medical device that received FDA 510(k) clearance on 2024-02-02. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K231373.
When did BD Vacutainer® K2 EDTA Blood Collection Tubes receive FDA 510(k) clearance?
BD Vacutainer® K2 EDTA Blood Collection Tubes received FDA 510(k) clearance on 2024-02-02, under 510(k) number K231373.
Who is the listed applicant for BD Vacutainer® K2 EDTA 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® K2 EDTA Blood Collection Tubes?
The FDA product code for BD Vacutainer® K2 EDTA Blood Collection Tubes is JKA.
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.
Related Devices (Code: JKA)
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.