Air Compression Recovery System— 510(k) K233536

Name: FDA 510(k) clearance K233536
Creator: U.S. Food and Drug Administration
Published: 2023-12-16

Substantially Equivalent

Shenzhen Dongjilian Medical Tech Co., Ltd.

FDA 510(k) clearance K233536 for Air Compression Recovery System, Substantially Equivalent on 2023-12-16. 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: 2023-11-03
Decision date: 2023-12-16
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.