Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System— 510(k) K173528

Name: FDA 510(k) clearance K173528
Creator: U.S. Food and Drug Administration
Published: 2018-02-06

Substantially Equivalent

Devon Medical Products (Jiangsu), Ltd.

FDA 510(k) clearance K173528 for Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System, Substantially Equivalent on 2018-02-06. Applicant: Devon Medical Products (Jiangsu), Ltd.. Device class: 2.

Clearance details

Applicant: Devon Medical Products (Jiangsu), Ltd.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2017-11-15
Decision date: 2018-02-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Nantong, CN

Download summary PDF View on FDA.gov ↗

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K172030 — Devon 512017-11-27
K170814 — Devon 242017-07-11

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