Air Compression Leg Massager (Models: S9036C, S9036B and S9036A)— 510(k) K222206

Name: FDA 510(k) clearance K222206
Creator: U.S. Food and Drug Administration
Published: 2022-09-30

Substantially Equivalent

Shenzhen Dongjilian Medical Tech Co., Ltd.

FDA 510(k) clearance K222206 for Air Compression Leg Massager (Models: S9036C, S9036B and S9036A), Substantially Equivalent on 2022-09-30. Applicant: Shenzhen Dongjilian Medical Tech Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Dongjilian Medical Tech Co., Ltd.
Product code: Code IRP
Device class: Class 2
Regulation: 21 CFR 890.5650
Advisory panel: Physical Medicine
Date received: 2022-07-25
Decision date: 2022-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.