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# Baxter Novum IQ Large Volume Pump Cleared
- URL: https://www.fdaweb.com/baxter-novum-iq-large-volume-pump-cleared/
- Published: 2024-04-01T12:00:00.000Z
- Updated: 2026-09-14T14:27:03.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5156673

FDA has cleared a Baxter International 510(k) clearance for its Novum IQ large volume infusion pump (LVP) with Dose IQ safety software. “Adding LVP modality to the Novum IQ Infusion Platform – which includes Baxter’s syringe infusion pump (SYR) with Dose IQ safety software, powered by the IQ Enterprise Connectivity Suite – enables clinicians to utilize a single, integrated system across a variety of patient care settings,” the company says. The device uses a common user interface that is designed to verify the association between a patient, medication and pump through a digital on-screen barcode. “The pump’s integrated experience also streamlines the training that clinicians need and helps reduce the cognitive burden associated with understanding how to properly operate multiple, disparate pump platforms,” Baxter says.