FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BD Texium™ Closed Male Luer

K Number: K223076 · Decision Mar 24, 2023
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
40
Applicant Total
34
Review Days
175

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Basic Information

Device Name
BD Texium™ Closed Male Luer
K Number
K223076
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Care Fusion
Date Received
September 30, 2022
Decision Date
March 24, 2023
Product Code
ONB
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ONB Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System

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Other Clearances by Care Fusion

K Number Device Name
K233021 BD SmartSite™ 13mm Vial Access Device; BD SmartSite™ 20mm Vial Access Device
K231888 BD Texium™ Needle-Free Syringe
K221327 BD Alaris™ Pump Infusion Sets
K221319 BD Alaris™ Pump Epidural Infusion Set
K223101 BD Secondary Infusion Set
K223088 BD SmartSite™ Needle-Free Connector
K201155 PleurX Peritoneal Catheter System
K170405 BD Curve Ascites Shunt
K171531 Jamshidi Bone Marrow Biopsy/Aspiration Needle, Jamshidi T-Handle Bone Marrow Biopsy/Aspiration Needle, Jamshidi Evolve Bone Marrow Biopsy/Aspiration Needle
K153748 AirLife Misty Finity Nebulizer
Search all 34 clearances from Care Fusion →