# K180248: VascuEase IC-1200-WH

- Pathway: 510(k) (Traditional)
- Applicant: Bio Compression Systems, Inc.
- Decided: Aug 7, 2018 after 190 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: 5 generations back to K915638 (1992). 21 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133274: Vena Pro, Innovamed Health, LLC (2014) Summary page 4.
- K131306: IC-1545-DL Multi Flo DVT Combo Intermittent Pneumatic Compression Device, Bio Compression Systems, Inc. (2013) Summary page 4.

## Most influential descendants
- K232270: DVT Motion Pneumatic Compression Device (2024), 0 descendants of its own

## Indications for use
VascuEase is a prescription device intended for the prophylaxis of Deep Vein Thrombosis (DVT), stimulating venous and arterial circulation, aiding in 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/K180248
Methodology: https://510kreport.com/methodology