LungProtect— 510(k) K240650

Substantially Equivalent

Traferox Technologies, Inc.

FDA 510(k) clearance K240650 for LungProtect, Substantially Equivalent on 2024-11-26. Applicant: Traferox Technologies, Inc..

Clearance details

Applicant: Traferox Technologies, Inc.
Product code: Code KDN
Advisory panel: Gastroenterology, Urology
Date received: 2024-03-07
Decision date: 2024-11-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga, CA

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