Air Compression Therapy Device— 510(k) K201694

Name: FDA 510(k) clearance K201694
Creator: U.S. Food and Drug Administration
Published: 2020-11-19

Substantially Equivalent

Shenzhen Dongjilian Electronics Co., Ltd.

FDA 510(k) clearance K201694 for Air Compression Therapy Device, Substantially Equivalent on 2020-11-19. Applicant: Shenzhen Dongjilian Electronics Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Dongjilian Electronics Co., Ltd.
Product code: Code IRP
Device class: Class 2
Regulation: 21 CFR 890.5650
Advisory panel: Physical Medicine
Date received: 2020-06-22
Decision date: 2020-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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K253919 — Cryo And Thermo Therapy System2026-06-10
K252396 — Cryo Sport 2.0 (AVA 501)2026-05-29

More clearances from Shenzhen Dongjilian Electronics Co., Ltd.

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K200354 — Electronic stimulator2020-06-29
K193354 — Air Compression Therapy Device2020-06-08

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