LymphaTech Mobile 3D Measuring Tool— 510(k) K261628

Name: FDA 510(k) clearance K261628
Creator: U.S. Food and Drug Administration
Published: 2026-10-28

Substantially Equivalent

Lymphatech, Inc.

FDA 510(k) clearance K261628 for LymphaTech Mobile 3D Measuring Tool, Substantially Equivalent on 2026-10-28. Applicant: Lymphatech, Inc.. Device class: 2.

Clearance details

Applicant: Lymphatech, Inc.
Product code: Product code OBH
Device class: Class 2
Regulation: 21 CFR 870.2770
Advisory panel: Cardiovascular
Date received: 2026-05-15
Decision date: 2026-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Atlanta, GA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code OBH

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K253224 — MySOZO Software version 6.0.1.2 (SW version 6.0.1.2)2026-01-28
K230530 — SOZO Pro2023-05-04
K220557 — MoistureMeterD Compact, LymphScanner2022-05-27
K180126 — SOZO2018-04-16
K172122 — SOZO2017-08-11

More clearances from Lymphatech, Inc.

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K251255 — LymphaTech Mobile 3D Measuring Tool2025-07-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.