Care Fusion is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Care Fusion - FDA 510(k) Cleared Devices
Recent clearances: BD SmartSite™ 13mm Vial Access Device, BD Texium™ Needle-Free Syringe, BD Alaris™ Pump Epidural Infusion Set
34
Total
29
Cleared
0
Denied
Care Fusion has 29 FDA 510(k) cleared medical devices. Based in Waukegan, US.
Latest FDA clearance: Mar 2024. Active since 2010.
Browse the FDA 510(k) cleared devices submitted by Care Fusion Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Care Fusion
34 devices
Cleared
Mar 06, 2024
BD SmartSite™ 13mm Vial Access Device
General Hospital
166d
Cleared
Sep 25, 2023
BD Texium™ Needle-Free Syringe
General Hospital
90d
Cleared
Jul 21, 2023
BD Alaris™ Pump Epidural Infusion Set
General Hospital
441d
Cleared
Jul 21, 2023
BD Alaris™ Pump Infusion Sets
General Hospital
441d
Cleared
May 12, 2023
BD Secondary Infusion Set
General Hospital
224d
Cleared
Apr 07, 2023
BD SmartSite™ Needle-Free Connector
General Hospital
189d
Cleared
Mar 24, 2023
BD Texium™ Closed Male Luer
General Hospital
175d
Cleared
Oct 21, 2020
PleurX Peritoneal Catheter System
Gastroenterology & Urology
174d
Cleared
Nov 02, 2017
BD Curve Ascites Shunt
Gastroenterology & Urology
265d
Cleared
Sep 11, 2017
Jamshidi Bone Marrow Biopsy/Aspiration Needle, Jamshidi T-Handle Bone Marrow...
Gastroenterology & Urology
109d
Cleared
May 17, 2017
AirLife Misty Finity Nebulizer
Anesthesiology
505d
Cleared
Nov 03, 2016
PleurX Peritoneal Catheter System
Gastroenterology & Urology
260d