# K181217: VesoFlow Lite DVT Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Caremed Supply, Inc.
- Decided: Aug 5, 2018 after 90 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). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141064: Vesoflow Plus DVT Compression Device, Caremed Supply, Inc. (2014) Summary page 4.

## Indications for use
The Caremed Supply Inc. VesoFlow Lite Deep Vein Thrombosis (DVT) Compression Device is intended to increase venous blood flow in at risk patients in order to help prevent deep vein thrombosis.

Source page: https://510kreport.com/device/K181217
Methodology: https://510kreport.com/methodology