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FDA 510(k)

NOxBOXi Nitric Oxide Delivery System

K-Number: K233251 · 2024-05-23

ApplicantLinde Gas & Equipment, Inc.
Decision Date2024-05-23
Product CodeMRN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NOxBOXi Nitric Oxide Delivery System is a medical device manufactured by Linde Gas & Equipment, Inc.. It received FDA 510(k) clearance on 2024-05-23 under approval number K233251. The device is classified under product code MRN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOxBOXi Nitric Oxide Delivery System?

NOxBOXi Nitric Oxide Delivery System is a medical device that received FDA 510(k) clearance on 2024-05-23. It is manufactured by Linde Gas & Equipment, Inc.. The 510(k) number is K233251.

When was NOxBOXi Nitric Oxide Delivery System approved by the FDA?

NOxBOXi Nitric Oxide Delivery System received FDA 510(k) clearance on 2024-05-23, under approval number K233251.

What company makes NOxBOXi Nitric Oxide Delivery System?

NOxBOXi Nitric Oxide Delivery System is manufactured by Linde Gas & Equipment, Inc..

What is the FDA product code for NOxBOXi Nitric Oxide Delivery System?

The FDA product code for NOxBOXi Nitric Oxide Delivery System is MRN.

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Other Devices by Linde Gas & Equipment, Inc.

K220898NOxBOXi Nitric Oxide Delivery System K231823NOxBOXi Nitric Oxide Delivery System

Related Devices (Code: MRN)

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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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