Devon 62 Deep Vein Thrombosis (DVT) Prevention Therapy Device— 510(k) K182578

Name: FDA 510(k) clearance K182578
Creator: U.S. Food and Drug Administration
Published: 2019-02-21

Substantially Equivalent

Devon Medical Products (Jiangsu), Ltd.

FDA 510(k) clearance K182578 for Devon 62 Deep Vein Thrombosis (DVT) Prevention Therapy Device, Substantially Equivalent on 2019-02-21. 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: 2018-09-19
Decision date: 2019-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nantong, CN

Download summary PDF View on FDA.gov ↗

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