Baxter Healthcare Corporation - FDA 510(k) Cleared Devices
61
Total
60
Cleared
1
Denied
Baxter Healthcare Corporation has 60 FDA 510(k) cleared medical devices. Based in Round Lake, US.
Latest FDA clearance: Dec 2025. Active since 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Baxter Healthcare Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Baxter Healthcare Corporation
61 devices
Cleared
Dec 16, 2025
Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)
Cardiovascular
193d
Cleared
Jul 28, 2025
Spectrum IQ Infusion System with Dose IQ Safety Software (3570009)
General Hospital
60d
Cleared
Jul 28, 2025
SIGMA Spectrum Infusion Pump with Master Drug Library
General Hospital
60d
Cleared
Mar 14, 2025
Solution Administration Sets
General Hospital
120d
Cleared
Feb 28, 2025
Intravascular Extension Sets and Accessories
General Hospital
205d
Cleared
Sep 05, 2024
Novum IQ Syringe Pump (40800BAXUS)
General Hospital
24d
Cleared
Aug 02, 2024
Actifuse ABX
Orthopedic
63d
Cleared
Mar 29, 2024
Novum IQ Large Volume Pump
General Hospital
1079d
Cleared
Mar 29, 2024
Dose IQ Safety Software
General Hospital
385d
Cleared
Sep 14, 2023
CleanCart A, CleanCart C, AK 98 Hemodialysis Machine
Gastroenterology & Urology
30d
Cleared
Mar 31, 2023
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library
General Hospital
86d
Cleared
Mar 31, 2023
Spectrum IQ Infusion System with Dose IQ Safety Software
General Hospital
84d
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