BD Texium Closed Male Luer
K-Number: K223076 · 2023-03-24
ApplicantCare Fusion
Decision Date2023-03-24
Product CodeONB
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
BD Texium Closed Male Luer is a medical device manufactured by Care Fusion. It received FDA 510(k) clearance on 2023-03-24 under approval number K223076. The device is classified under product code ONB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Care Fusion. The 510(k) number is K223076.
When was BD Texium Closed Male Luer approved by the FDA?
BD Texium Closed Male Luer received FDA 510(k) clearance on 2023-03-24, under approval number K223076.
What company makes BD Texium Closed Male Luer?
BD Texium Closed Male Luer is manufactured by Care Fusion.
What is the FDA product code for BD Texium Closed Male Luer?
The FDA product code for BD Texium Closed Male Luer is ONB.
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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.