10:26 AM EDT, 04/01/2024 (MT Newswires) -- Baxter International ( BAX ) said Monday its Novum IQ large volume infusion pump, equipped with Dose IQ safety software, has received FDA 510(k) clearance from the US Food and Drug Administration.

The company said the Novum IQ's LVP modality allows the administration of high-volume infusions at faster rates.

The FDA clearance allows Baxter to offer an integrated infusion system, combining large volume and syringe pumps with advanced digital health solutions for improved patient safety and clinical efficiency, the company said.

The Novum IQ LVP and Novum IQ SYR are now available to order in the US, Baxter said.

Shares of Baxter were up more than 2% in recent Monday trading.

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