Compression Therapy Device— 510(k) K191856

Name: FDA 510(k) clearance K191856
Creator: U.S. Food and Drug Administration
Published: 2020-03-19

Substantially Equivalent

Guangzhou Longest Science & Technology Co., Ltd.

FDA 510(k) clearance K191856 for Compression Therapy Device, Substantially Equivalent on 2020-03-19. Applicant: Guangzhou Longest Science & Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Guangzhou Longest Science & Technology Co., Ltd.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2019-07-11
Decision date: 2020-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Guangzhou, CN

Download summary PDF View on FDA.gov ↗

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K191862 — Compression Therapy Device Model LGT-2200SP2019-10-29
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