BD VACUTAINER PLUS PST II TUBE
K-Number: K022130 · 2002-07-29
Advertisement
Device Summary
Frequently Asked Questions
What is the BD VACUTAINER PLUS PST II TUBE?
BD VACUTAINER PLUS PST II TUBE is a medical device that received FDA 510(k) clearance on 2002-07-29. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K022130.
When did BD VACUTAINER PLUS PST II TUBE receive FDA 510(k) clearance?
BD VACUTAINER PLUS PST II TUBE received FDA 510(k) clearance on 2002-07-29, under 510(k) number K022130.
Who is the listed applicant for BD VACUTAINER PLUS PST II TUBE?
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 PLUS PST II TUBE?
The FDA product code for BD VACUTAINER PLUS PST II TUBE 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.
Advertisement