Devon 52 Sequential Compression Device— 510(k) K182150

Name: FDA 510(k) clearance K182150
Creator: U.S. Food and Drug Administration
Published: 2018-12-18

Substantially Equivalent

Devon Medical Products (Jiangsu), Ltd.

FDA 510(k) clearance K182150 for Devon 52 Sequential Compression Device, Substantially Equivalent on 2018-12-18. 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: 2018-08-08
Decision date: 2018-12-18
Decision: Substantially Equivalent
Clearance type: Special
Location: Nantong, CN

Download summary PDF View on FDA.gov ↗

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