# K250242: Compression Therapy Device (LGT-2202DVT)

- Pathway: 510(k) (Traditional)
- Applicant: Guangzhou Longest Medical Technology Co., Ltd.
- Decided: Apr 24, 2026 after 452 days
- Product code: JOW (Sleeve, Limb, Compressible)
- Device class: 2
- Regulation: 21 CFR 870.5800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K953648 (1996). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120944: Kendall SCD 700 Sequential Compression Controller, Covidien (2012) Summary page 5.
- K141064: Vesoflow Plus DVT Compression Device, Caremed Supply, Inc. (2014) Summary page 8.

## Indications for use
1. Leg Compression with sleeve is indicated for: - Deep Vein Thrombosis and pulmonary embolism prophylaxis 2. Foot Compression with sleeve is indicated for: - Circulation enhancement - Deep Vein Thrombosis prophylaxis - Edema - Acute - Edema - Chronic - Extremity pain incident to trauma or surgery - Leg Ulcers - Venous stasis / venous insufficiency The Compression Therapy Device is designed to be used in patients over 22 years old.

Source page: https://510kreport.com/device/K250242
Methodology: https://510kreport.com/methodology