Compression Therapy Device Model LGT-2200SP— 510(k) K191862

Name: FDA 510(k) clearance K191862
Creator: U.S. Food and Drug Administration
Published: 2019-10-29

Substantially Equivalent

Guangzhou Longest Science & Technology Co., Ltd.

FDA 510(k) clearance K191862 for Compression Therapy Device Model LGT-2200SP, Substantially Equivalent on 2019-10-29. Applicant: Guangzhou Longest Science & Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Guangzhou Longest Science & Technology Co., Ltd.
Product code: Code IRP
Device class: Class 2
Regulation: 21 CFR 890.5650
Advisory panel: Physical Medicine
Date received: 2019-07-11
Decision date: 2019-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Guangzhou, CN

Download summary PDF View on FDA.gov ↗

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