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FDA 510(k)

Compression Therapy Device Model LGT-2200SP

K-Number: K191862 · 2019-10-29

ApplicantGuangzhou Longest Science & Technology Co., Ltd.
Decision Date2019-10-29
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Compression Therapy Device Model LGT-2200SP is a medical device manufactured by Guangzhou Longest Science & Technology Co., Ltd.. It received FDA 510(k) clearance on 2019-10-29 under approval number K191862. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Compression Therapy Device Model LGT-2200SP?

Compression Therapy Device Model LGT-2200SP is a medical device that received FDA 510(k) clearance on 2019-10-29. It is manufactured by Guangzhou Longest Science & Technology Co., Ltd.. The 510(k) number is K191862.

When was Compression Therapy Device Model LGT-2200SP approved by the FDA?

Compression Therapy Device Model LGT-2200SP received FDA 510(k) clearance on 2019-10-29, under approval number K191862.

What company makes Compression Therapy Device Model LGT-2200SP?

Compression Therapy Device Model LGT-2200SP is manufactured by Guangzhou Longest Science & Technology Co., Ltd..

What is the FDA product code for Compression Therapy Device Model LGT-2200SP?

The FDA product code for Compression Therapy Device Model LGT-2200SP is IRP.

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Related PubMed Literature

PMID: 41915420 Analysis Model for Infant Incubator Adverse Events Using Retrieval-Augmented Generation Combined With Dual-Adapter Fine-Tuning: Development and Evaluation Study. JMIR medical informatics (2026) PMID: 41831468 Cardiometabolic prediction models for young people with psychosis spectrum disorders in the UK (PsyMetRiC 2.0): a retrospective, multicohort clinical prediction model study. The lancet. Psychiatry (2026) PMID: 41501972 First Application of an Eddy-Scale Hemolysis Model to the Food and Drug Administration Nozzle Using Computational Fluid Dynamics. ASAIO journal (American Society for Artificial Internal Organs : 1992) (2026) PMID: 41072144 Use of Bayesian decision analysis in the design of patient-centered clinical trials for kidney failure devices. Computers in biology and medicine (2025)

Other Devices by Guangzhou Longest Science & Technology Co., Ltd.

K182108Portable Electro-Stimulation Therapy Device K201845Portable Electro-Stimulation Therapy Device, Model: LGT-232(US) K182020Portable Electro-Stimulation Therapy Device K191856Compression Therapy Device K202110MStim Drop Model: LGT-233

Related Devices (Code: IRP)

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Official Source

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

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