# K101523: Circuflow 5200 Sequential Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Devon Medical, Inc.
- Decided: Jun 17, 2010 after 15 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: 2 generations back to K043423 (2005). 3 ancestors in all.
21 later devices descend from it; 5 cite it directly.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100446: Circuflow 5100 Sequential Compression Device, Devon Medical, Inc. (2010) Summary page 1.
- K050584: GS-128 Gradient Compression System, Medmark Technologies, LLC (2005) Summary page 1.

## Most influential descendants
- K123647: Circuflow 5208 Sequential Compression Device (2013), 12 descendants of its own
- K123959: Circuflow 5150 (2013), 6 descendants of its own
- K143185: entré Model PD08-U (2015), 4 descendants of its own
- K183631: medi pneumatic compression system (pcs) – brio (Model 651) (2019), 3 descendants of its own
- K172770: AIROS 6 Sequential Compression Device (2018), 3 descendants of its own

## Indications for use
The CircuFlow 5200 Sequential Compression Device is a compression device based on sequential pneumatic compression technique which is intended for the treatment of the following conditions: Lymph edema Venous stasis ulcers Venous insufficiency Peripheral edema The device is intended for home and hospital use.

Source page: https://510kreport.com/device/K101523
Methodology: https://510kreport.com/methodology