Care Fusion is one of 12929 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.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Vyaire Medical.
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