BD Texium™ Closed Male Luer
K-Number: K223076 · 2023-03-24
Device Summary
Frequently Asked Questions
What is the BD Texium™ Closed Male Luer?
BD Texium™ Closed Male Luer is a medical device that received FDA 510(k) clearance on 2023-03-24. The listed applicant is Care Fusion. The 510(k) number is K223076.
When did BD Texium™ Closed Male Luer receive FDA 510(k) clearance?
BD Texium™ Closed Male Luer received FDA 510(k) clearance on 2023-03-24, under 510(k) number K223076.
Who is the listed applicant for BD Texium™ Closed Male Luer?
The FDA 510(k) record lists Care Fusion as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BD Texium™ Closed Male Luer?
The FDA product code for BD Texium™ Closed Male Luer is ONB.
Other records listing Care Fusion 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: ONB)
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.