# K172030: Devon 51

- Pathway: 510(k) (Traditional)
- Applicant: Devon Medical Products (Jiangsu), Ltd.
- Decided: Nov 27, 2017 after 145 days
- Product code: JOW (Sleeve, Limb, Compressible)
- Device class: 2
- Regulation: 21 CFR 870.5800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K043423 (2005). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101523: Circuflow 5200 Sequential Compression Device, Devon Medical, Inc. (2010) Summary page 4.

## Indications for use
The Devon 51 Series Sequential Compression Device is a compression device based on sequential pneumatic Compression technique which is intended for the treatment of the following conditions: - Lymphedema - Venous stasis ulcers - Venous insufficiency - Peripheral edema The device is intended for both home and hospital use.

Source page: https://510kreport.com/device/K172030
Methodology: https://510kreport.com/methodology