Care Fusion

FDA Regulatory Profile

Care Fusion appears in FDA public data with 0 recalls, 34 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 6, 2024.

Summary

Total Recalls
0
510(k) Clearances
34
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K233021BD SmartSite™ 13mm Vial Access Device; BD SmartSite™ 20mm Vial Access DeviceMarch 6, 2024
K231888BD Texium™ Needle-Free SyringeSeptember 25, 2023
K221327BD Alaris™ Pump Infusion SetsJuly 21, 2023
K221319BD Alaris™ Pump Epidural Infusion SetJuly 21, 2023
K223101BD Secondary Infusion SetMay 12, 2023
K223088BD SmartSite™ Needle-Free ConnectorApril 7, 2023
K223076BD Texium™ Closed Male LuerMarch 24, 2023
K201155PleurX Peritoneal Catheter SystemOctober 21, 2020
K170405BD Curve Ascites ShuntNovember 2, 2017
K171531Jamshidi Bone Marrow Biopsy/Aspiration Needle, Jamshidi T-Handle Bone Marrow Biopsy/Aspiration NeedlSeptember 11, 2017
K153748AirLife Misty Finity NebulizerMay 17, 2017
K160437PleurX Peritoneal Catheter SystemNovember 3, 2016
K160450Pleurx Pleural Catheter SystemOctober 31, 2016
K151303AirLife Infant Heated Wire CircuitJanuary 21, 2016
K151125AVAflex Vertebral Balloon SystemNovember 24, 2015
K150523AVAmax Vertebral BalloonOctober 29, 2015
K141965PLEURX PLEURAL CATHETER SYSTEM, PLEURX CATHETER ACCESS KITJuly 2, 2015
K141722CAREFUSION GOLD TISSUE MARKERJanuary 23, 2015
K143234MaxZero Administration SetsNovember 20, 2014
K141552ACHIEVE PROGRAMMABLE AUOMATED BIOPSY SYSTEMSSeptember 5, 2014