# K080134: Compressible Limb and Circulation Therapy System, Model WHF-314 (Power-Q1000)

- Pathway: 510(k) (Traditional)
- Applicant: Wonjin Mulsan Co., Ltd.
- Decided: Jan 23, 2009 after 371 days
- Product code: IRP (Massager, Powered Inflatable Tube)
- Device class: 2
- Regulation: 21 CFR 890.5650
- 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 K914774 (1992). 3 ancestors in all.
14 later devices descend from it; 1 cites it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K915638: Talley TM200 Intermttent Compression Unit, Progressive Medical Technology, Inc. (1992) Summary page 1.
- K013061: Biotouch Massage Therapy System, Tactile Systems Technology, Inc. (2002)

## Most influential descendants
- K100656: Compressible Limb Therapy System Model WHF-324 (Power-Q1000 Plus) (2010), 13 descendants of its own
- K102320: Compressible Limb and Circulation Therapy System Model LX7(V7) (2011), 6 descendants of its own
- K113275: Compressible Limb Therapy System (2012), 3 descendants of its own
- K102319: Compressible Limb and Circulation Therapy System Model Wic-2008 (2011), 3 descendants of its own
- K161907: Pressure Therapy System (2017), 1 descendant of its own

## Indications for use
The WHF-314 (POWER Q1000) device is intended for use by medical professionals and patients at home, who are under medical supervision, in treating many conditions, such as Primary lymphedema, Edema following trauma and sport injuries, Post immobilization edema, Venous insufficiencies, Lymphedema

Source page: https://510kreport.com/device/K080134
Methodology: https://510kreport.com/methodology