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FDA 510(k)

Novum IQ Syringe Pump (40800BAXUS)

K-Number: K242390 · 2024-09-05

ApplicantBaxter Healthcare Corporation
Decision Date2024-09-05
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Novum IQ Syringe Pump (40800BAXUS) is a medical device manufactured by Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2024-09-05 under approval number K242390. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Novum IQ Syringe Pump (40800BAXUS)?

Novum IQ Syringe Pump (40800BAXUS) is a medical device that received FDA 510(k) clearance on 2024-09-05. It is manufactured by Baxter Healthcare Corporation. The 510(k) number is K242390.

When was Novum IQ Syringe Pump (40800BAXUS) approved by the FDA?

Novum IQ Syringe Pump (40800BAXUS) received FDA 510(k) clearance on 2024-09-05, under approval number K242390.

What company makes Novum IQ Syringe Pump (40800BAXUS)?

Novum IQ Syringe Pump (40800BAXUS) is manufactured by Baxter Healthcare Corporation.

What is the FDA product code for Novum IQ Syringe Pump (40800BAXUS)?

The FDA product code for Novum IQ Syringe Pump (40800BAXUS) is FRN.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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