LungProtect
K-Number: K240650 · 2024-11-26
Device Summary
Frequently Asked Questions
What is the LungProtect?
LungProtect is a medical device that received FDA 510(k) clearance on 2024-11-26. The listed applicant is Traferox Technologies, Inc.. The 510(k) number is K240650.
When did LungProtect receive FDA 510(k) clearance?
LungProtect received FDA 510(k) clearance on 2024-11-26, under 510(k) number K240650.
Who is the listed applicant for LungProtect?
The FDA 510(k) record lists Traferox Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LungProtect?
The FDA product code for LungProtect is KDN.
Other records listing Traferox Technologies, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KDN)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.