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FDA 510(k)

LungProtect

K-Number: K240650 · 2024-11-26

ApplicantTraferox Technologies, Inc.
Decision Date2024-11-26
Product CodeKDN
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LungProtect is a medical device manufactured by Traferox Technologies, Inc.. It received FDA 510(k) clearance on 2024-11-26 under approval number K240650. The device is classified under product code KDN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LungProtect?

LungProtect is a medical device that received FDA 510(k) clearance on 2024-11-26. It is manufactured by Traferox Technologies, Inc.. The 510(k) number is K240650.

When was LungProtect approved by the FDA?

LungProtect received FDA 510(k) clearance on 2024-11-26, under approval number K240650.

What company makes LungProtect?

LungProtect is manufactured by Traferox Technologies, Inc..

What is the FDA product code for LungProtect?

The FDA product code for LungProtect is KDN.

Other Devices by Traferox Technologies, Inc.

K243870X°Port Lung Preservation System; X°Port Lung Preservation Solution

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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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