Compression Therapy Device Model LGT-2200SP

FDA 510(k) K191862 · Guangzhou Longest Science & Technology Co., Ltd.

Substantially Equivalent

510(k) numberK191862

Submission

Device name
Compression Therapy Device Model LGT-2200SP
Applicant
Guangzhou Longest Science & Technology Co., Ltd.
Guangzhou, CN
Received
July 11, 2019
Decision date
October 29, 2019
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
IRP – Massager, Powered Inflatable Tube
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5650
Specialty
Physical Medicine

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Questions and answers

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

Compression Therapy Device Model LGT-2200SP (K191862) received a 510(k) decision of Substantially Equivalent on October 29, 2019, 110 days after the submission was received.

What is the product code of K191862?

The FDA product code is IRP – Massager, Powered Inflatable Tube, a Class II (moderate risk) device regulated under 21 CFR 890.5650.