# K141390: Intermittent Pneumatic Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Wuhan Landing Medical Hi-Tech, Ltd.
- Decided: Nov 18, 2014 after 175 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: 4 generations back to K953648 (1996). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123830: Intermittent Pneumatic Compression Device, Dalian Labtek Science & Development Co., Ltd. (2013) Summary page 5.

## Indications for use
The LD Q-IPC III is a system to prevent DVT(Deep Vein Thrombosis) by improving the blood velocity of patients. Leg Compression The use of the product with Calf Cuff and Thigh Cuff is indicated for: 1. Deep vein thrombosis and pulmonary embolism prophylaxis. Foot Compression The use of the product with Foot Cuff is indicated for: 1. Circulation enhancement. 2. Deep vein thrombosis prophylaxis. 3. Edema-Acute. 4. Edema-Chronic. 5. Extremity pain incident to trauma or surgery. 6. Leg Ulcers. 7. Venous stasis /Venous insufficiency.

Source page: https://510kreport.com/device/K141390
Methodology: https://510kreport.com/methodology