Compression Therapy Device (LGT-2202DVT)— 510(k) K250242

Name: FDA 510(k) clearance K250242
Creator: U.S. Food and Drug Administration
Published: 2026-04-24

Substantially Equivalent

Guangzhou Longest Medical Technology Co., Ltd.

FDA 510(k) clearance K250242 for Compression Therapy Device (LGT-2202DVT), Substantially Equivalent on 2026-04-24. Applicant: Guangzhou Longest Medical Technology Co., Ltd.. Device class: 2.

Summary

Guangzhou Longest Medical Technology's Compression Therapy Device (model LGT-2202DVT) is filed under product code JOW (Sleeve, Limb, Compressible).

Class II, 21 CFR 870.5800. Cardiovascular is both the classification panel and the review panel, and it came in as a Traditional 510(k).

Guangzhou Longest Medical Technology filed from Guangzhou, China. The decision came 452 calendar days after FDA received it (January 27, 2025 to April 24, 2026).

Clearance details

Applicant: Guangzhou Longest Medical Technology Co., Ltd.
Product code: Product code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2025-01-27
Decision date: 2026-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Guangzhou, CN

Download summary PDF View on FDA.gov ↗

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