BD VACUTAINER SST II PLUS TUBES
K-Number: K023331 · 2002-11-25
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Device Summary
Frequently Asked Questions
What is the BD VACUTAINER SST II PLUS TUBES?
BD VACUTAINER SST II PLUS TUBES is a medical device that received FDA 510(k) clearance on 2002-11-25. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K023331.
When did BD VACUTAINER SST II PLUS TUBES receive FDA 510(k) clearance?
BD VACUTAINER SST II PLUS TUBES received FDA 510(k) clearance on 2002-11-25, under 510(k) number K023331.
Who is the listed applicant for BD VACUTAINER SST II PLUS TUBES?
The FDA 510(k) record lists Becton, Dickinson & CO as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD VACUTAINER SST II PLUS TUBES?
The FDA product code for BD VACUTAINER SST II PLUS 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 & CO 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.
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