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FDA 510(k)

Noxturnal Web

K-Number: K241288 · 2024-12-23

ApplicantNox Medical Ehf
Decision Date2024-12-23
Product CodeOLV
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Noxturnal Web is a medical device manufactured by Nox Medical Ehf. It received FDA 510(k) clearance on 2024-12-23 under approval number K241288. The device is classified under product code OLV. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Noxturnal Web?

Noxturnal Web is a medical device that received FDA 510(k) clearance on 2024-12-23. It is manufactured by Nox Medical Ehf. The 510(k) number is K241288.

When was Noxturnal Web approved by the FDA?

Noxturnal Web received FDA 510(k) clearance on 2024-12-23, under approval number K241288.

What company makes Noxturnal Web?

Noxturnal Web is manufactured by Nox Medical Ehf.

What is the FDA product code for Noxturnal Web?

The FDA product code for Noxturnal Web is OLV.

Other Devices by Nox Medical Ehf

K252330DeepRESP K241960DeepRESP K260585Noxturnal Web

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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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