Baxter Healthcare Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Baxter Healthcare Corporation - FDA 510(k) Cleared Devices
Recent clearances: Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs), Spectrum IQ Infusion System with Dose IQ Safety Software (3570009), SIGMA Spectrum Infusion Pump with Master Drug Library
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.
Regulatory submissions have been managed by Regulatory Technology Services, LLC, Gambro Industries and Gambro Dasco Spa.
FDA 510(k) Regulatory Record - Baxter Healthcare Corporation
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