# K232270: DVT Motion Pneumatic Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Koge Micro Tech Co., Ltd.
- Decided: Mar 6, 2024 after 219 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: 6 generations back to K915638 (1992). 22 ancestors in all.
No later device cites it as a predicate yet.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180248: VascuEase IC-1200-WH, Bio Compression Systems, Inc. (2018) Summary page 4.

## Indications for use
DVT Motion Pneumatic Compression Device is a prescription device intended for prophylaxis of Deep Vein Thrombosis (DVT), stimulating venous and arterial circulation, aiding in the prevention of venous stasis ulcers, aiding in the healing of cutaneous ulcers, reducing acute/chronic edema and compartmental pressures. For use in home or hospital setting.

Source page: https://510kreport.com/device/K232270
Methodology: https://510kreport.com/methodology