Devon 24D Deep Vein Thrombosis (DVT) Prevention Therapy System— 510(k) K190423

Name: FDA 510(k) clearance K190423
Creator: U.S. Food and Drug Administration
Published: 2019-03-19

Substantially Equivalent

Devon Medical Products (Jiangsu), Ltd.

FDA 510(k) clearance K190423 for Devon 24D Deep Vein Thrombosis (DVT) Prevention Therapy System, Substantially Equivalent on 2019-03-19. 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: 2019-02-22
Decision date: 2019-03-19
Decision: Substantially Equivalent
Clearance type: Special
Location: Nantong, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code JOW

view all

K261807 — Sequential Circulator (SC-4004-DL, SC-4008-DL)2026-09-11
K254217 — Aerloom2026-08-31
K253555 — Flexitouch® Plus Advanced Pneumatic Compression System2026-07-31
K253386 — DVT Garment2026-06-25
K250242 — Compression Therapy Device (LGT-2202DVT)2026-04-24

More clearances from Devon Medical Products (Jiangsu), Ltd.

view all

K182578 — Devon 62 Deep Vein Thrombosis (DVT) Prevention Therapy Device2019-02-21
K182150 — Devon 52 Sequential Compression Device2018-12-18
K173528 — Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy System2018-02-06
K172030 — Devon 512017-11-27
K170814 — Devon 242017-07-11

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