# K123959: Circuflow 5150

- Pathway: 510(k) (Traditional)
- Applicant: Devon Medical, Inc.
- Decided: Feb 28, 2013 after 69 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.
6 later devices descend from it; 2 cite it directly.
0 of 11 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 1.
- K100446: Circuflow 5100 Sequential Compression Device, Devon Medical, Inc. (2010) Summary page 1.

## Most influential descendants
- K143185: entré Model PD08-U (2015), 4 descendants of its own
- K254217: Aerloom (2026), 0 descendants of its own
- K250817: Coretech Compression System (Coretech RHB3003) (2025), 0 descendants of its own
- K234155: Nimbl (model PD08-N1) (2024), 0 descendants of its own
- K212287: Dayspring Lite (2021), 0 descendants of its own

## Indications for use
The CircuFlowm 5150 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/K123959
Methodology: https://510kreport.com/methodology