# K101915: Vasopress Supreme Mini Model VP500DM

- Pathway: 510(k) (Special)
- Applicant: Compression Therapy Concepts, Inc.
- Decided: Aug 6, 2010 after 28 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K143202: ANGIO-PRESS DVT Compression Device Model Name: IPCS (2015), 1 descendant of its own
- K173012: ANGIO-PRESS LITE DVT Compression Device (2018), 0 descendants of its own

## Indications for use
The VasoPress Pump (Model VPSOODM) is an external pneumatic compression device for use with VasoPress DVT garments, and is intended to lower the risk of deep vein thrombosis (DVT) in patients who may be at risk.

Source page: https://510kreport.com/device/K101915
Methodology: https://510kreport.com/methodology