Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Compression Therapy Device (LGT-2202DVT)

K-Number: K250242 · 2026-04-24

Decision Date2026-04-24
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Compression Therapy Device (LGT-2202DVT) is a medical device manufactured by Guangzhou Longest Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-04-24 under approval number K250242. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Compression Therapy Device (LGT-2202DVT)?

Compression Therapy Device (LGT-2202DVT) is a medical device that received FDA 510(k) clearance on 2026-04-24. It is manufactured by Guangzhou Longest Medical Technology Co., Ltd.. The 510(k) number is K250242.

When was Compression Therapy Device (LGT-2202DVT) approved by the FDA?

Compression Therapy Device (LGT-2202DVT) received FDA 510(k) clearance on 2026-04-24, under approval number K250242.

What company makes Compression Therapy Device (LGT-2202DVT)?

Compression Therapy Device (LGT-2202DVT) is manufactured by Guangzhou Longest Medical Technology Co., Ltd..

What is the FDA product code for Compression Therapy Device (LGT-2202DVT)?

The FDA product code for Compression Therapy Device (LGT-2202DVT) is JOW.

Related Clinical Trials

Related PubMed Literature

Other Devices by Guangzhou Longest Medical Technology Co., Ltd.

Related Devices (Code: JOW)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.