# K141064: Vesoflow Plus DVT Compression Device

- Pathway: 510(k) (Traditional)
- Applicant: Caremed Supply, Inc.
- Decided: Dec 4, 2014 after 224 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: 3 generations back to K953648 (1996). 5 ancestors in all.
4 later devices descend from it; 3 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110977: Vesoflow, Caremed Supply, Inc. (2011) Summary page 4.

## Most influential descendants
- K200154: B&J DVT Compression Devices MHH800/MHH800SQ (2020), 1 descendant of its own
- K250242: Compression Therapy Device (LGT-2202DVT) (2026), 0 descendants of its own
- K231801: MedHealth DVT compression Devices MHH900S/MHH900E (2023), 0 descendants of its own
- K181217: VesoFlow Lite DVT Compression Device (2018), 0 descendants of its own

## Indications for use
The Caremed Supply Inc. VESOFLOW PLUS SQS and IPCS Deep Vein Thrombosis (DVT) Compression Devices are intended to increase venous blood flow in at risk patients in order to help prevent deep vein thrombosis.

Source page: https://510kreport.com/device/K141064
Methodology: https://510kreport.com/methodology