Compression Therapy Device (LGT-2210DS)— 510(k) K250244

Name: FDA 510(k) clearance K250244
Creator: U.S. Food and Drug Administration
Published: 2025-07-25

Substantially Equivalent

Guangzhou Longest Medical Technology Co., Ltd.

FDA 510(k) clearance K250244 for Compression Therapy Device (LGT-2210DS), Substantially Equivalent on 2025-07-25. Applicant: Guangzhou Longest Medical Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Guangzhou Longest Medical Technology Co., Ltd.
Product code: Code IRP
Device class: Class 2
Regulation: 21 CFR 890.5650
Advisory panel: Physical Medicine
Date received: 2025-01-27
Decision date: 2025-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Guanzhou, CN

Download summary PDF View on FDA.gov ↗

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