LymphaTech Mobile 3D Measuring Tool— 510(k) K251255

Name: FDA 510(k) clearance K251255
Creator: U.S. Food and Drug Administration
Published: 2025-07-22

Substantially Equivalent

Lymphatech, Inc.

FDA 510(k) clearance K251255 for LymphaTech Mobile 3D Measuring Tool, Substantially Equivalent on 2025-07-22. Applicant: Lymphatech, Inc.. Device class: 1.

Clearance details

Applicant: Lymphatech, Inc.
Product code: Code SFG
Device class: Class 1
Regulation: 21 CFR 878.4160
Advisory panel: General, Plastic Surgery
Date received: 2025-04-23
Decision date: 2025-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Atlanta, GA, US

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